Linked Data
ClinVar Variation Id:
127751
ClinVar RCV Id:
RCV000115647
RCV000121835
RCV000415644
RCV000586586
RCV001249992
RCV001798333
RCV003492485
RCV001080700
RCV001354576
RCV003389688
dbSNP Id:
rs200513014
ExAC:
7:6029571 T / C
gnomAD v2:
7-6029571-T-C
gnomAD v3:
7-5989940-T-C
gnomAD v4:
7-5989940-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5989940T>C , CM000669.2:g.5989940T>C | GRCh38 |
| NC_000007.13:g.6029571T>C , CM000669.1:g.6029571T>C | GRCh37 |
| NC_000007.12:g.5996097T>C | NCBI36 |
| NG_008466.1:g.24167A>G , LRG_161:g.24167A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*400A>G | ENSP00000514615.2:n.*400A>G | |
| ENST00000699840.2:c.1001A>G | ENSP00000514638.2:p.Asn334Ser | |
| ENST00000699930.2:c.896A>G | ENSP00000514695.2:p.Asn299Ser | |
| ENST00000406569.8:c.1004A>G | ENSP00000514464.1:p.Asn335Ser | |
| ENST00000644110.2:c.*598A>G | ENSP00000496392.2:n.*598A>G | |
| ENST00000699752.1:c.988+2033A>G | ENSP00000514561.1:n.988+2033A>G | |
| ENST00000699753.1:c.*425A>G | ENSP00000514562.1:n.*425A>G | |
| ENST00000699754.1:c.806A>G | ENSP00000514563.1:p.Asn269Ser | |
| ENST00000699755.1:c.*403A>G | ENSP00000514564.1:n.*403A>G | |
| ENST00000699756.1:c.*591A>G | ENSP00000514565.1:n.*591A>G | |
| ENST00000699757.1:c.*261A>G | ENSP00000514566.1:n.*261A>G | |
| ENST00000699758.1:c.*261A>G | ENSP00000514567.1:n.*261A>G | |
| ENST00000699759.1:n.1858A>G | ||
| ENST00000699760.1:c.686A>G | ENSP00000514568.1:p.Asn229Ser | |
| ENST00000699761.1:c.599A>G | ENSP00000514569.1:p.Asn200Ser | |
| ENST00000699762.1:c.431A>G | ENSP00000514570.1:p.Asn144Ser | |
| ENST00000699763.1:c.*94A>G | ENSP00000514571.1:n.*94A>G | |
| ENST00000699764.1:c.1004A>G | ENSP00000514572.1:p.Asn335Ser | |
| ENST00000699765.1:c.*100A>G | ENSP00000514573.1:n.*100A>G | |
| ENST00000699766.1:c.1004A>G | ENSP00000514574.1:p.Asn335Ser | |
| ENST00000699767.1:c.1004A>G | ENSP00000514575.1:p.Asn335Ser | |
| ENST00000699768.1:c.1004A>G | ENSP00000514576.1:p.Asn335Ser | |
| ENST00000699811.1:c.599A>G | ENSP00000514614.1:p.Asn200Ser | |
| ENST00000699813.1:n.1117A>G | ||
| ENST00000699814.1:c.627A>G | ||
| ENST00000699815.1:c.*496A>G | ENSP00000514616.1:n.*496A>G | |
| ENST00000699816.1:c.599A>G | ENSP00000514617.1:p.Asn200Ser | |
| ENST00000699817.1:c.*598A>G | ENSP00000514618.1:n.*598A>G | |
| ENST00000699818.1:c.599A>G | ENSP00000514619.1:p.Asn200Ser | |
| ENST00000699819.1:c.*161A>G | ENSP00000514620.1:n.*161A>G | |
| ENST00000699820.1:c.1004A>G | ENSP00000514621.1:p.Asn335Ser | |
| ENST00000699821.1:c.599A>G | ENSP00000514622.1:p.Asn200Ser | |
| ENST00000699822.1:c.*456A>G | ENSP00000514623.1:n.*456A>G | |
| ENST00000699823.1:c.599A>G | ENSP00000514624.1:p.Asn200Ser | |
| ENST00000699824.1:c.*507A>G | ENSP00000514625.1:n.*507A>G | |
| ENST00000699825.1:c.583+2033A>G | ENSP00000514626.1:n.583+2033A>G | |
| ENST00000699826.1:c.*403A>G | ENSP00000514627.1:n.*403A>G | |
| ENST00000699827.1:c.836A>G | ENSP00000514628.1:p.Asn279Ser | |
| ENST00000699828.1:c.*94A>G | ENSP00000514629.1:n.*94A>G | |
| ENST00000699829.1:c.*505A>G | ENSP00000514630.1:n.*505A>G | |
| ENST00000699830.1:c.*403A>G | ENSP00000514631.1:n.*403A>G | |
| ENST00000699833.1:n.2776A>G | ||
| ENST00000699837.1:c.599A>G | ENSP00000514635.1:p.Asn200Ser | |
| ENST00000699838.1:c.*904A>G | ENSP00000514636.1:n.*904A>G | |
| ENST00000699839.1:c.1190A>G | ENSP00000514637.1:p.Asn397Ser | |
| ENST00000699840.1:c.1001A>G | ENSP00000514638.1:p.Asn334Ser | |
| ENST00000699916.1:c.*261A>G | ENSP00000514684.1:n.*261A>G | |
| ENST00000699917.1:c.*453A>G | ENSP00000514685.1:n.*453A>G | |
| ENST00000699918.1:c.*505A>G | ENSP00000514686.1:n.*505A>G | |
| ENST00000699919.1:c.*591A>G | ENSP00000514687.1:n.*591A>G | |
| ENST00000699920.1:c.*640A>G | ENSP00000514688.1:n.*640A>G | |
| ENST00000699928.1:c.988+2033A>G | ENSP00000514693.1:n.988+2033A>G | |
| ENST00000699929.1:c.*305A>G | ENSP00000514694.1:n.*305A>G | |
| ENST00000699930.1:c.896A>G | ENSP00000514695.1:p.Asn299Ser | |
| ENST00000699931.1:n.2432A>G | ||
| ENST00000699932.1:c.*222A>G | ENSP00000514696.1:n.*222A>G | |
| ENST00000699933.1:n.984A>G | ||
| ENST00000699951.1:c.*100A>G | ENSP00000514706.1:n.*100A>G | |
| ENST00000699952.1:c.803+7386A>G | ENSP00000514707.1:n.803+7386A>G | |
| ENST00000699953.1:c.*111A>G | ENSP00000514708.1:n.*111A>G | |
| ENST00000699954.1:c.*305A>G | ENSP00000514709.1:n.*305A>G | |
| ENST00000265849.12:c.1004A>G MANE Select | ENSP00000265849.7:p.Asn335Ser | |
| ENST00000642292.1:c.599A>G | ENSP00000495524.1:p.Asn200Ser | |
| ENST00000642456.1:c.599A>G | ENSP00000493814.1:p.Asn200Ser | |
| ENST00000643595.1:c.*403A>G | ENSP00000494497.1:n.*403A>G | |
| ENST00000644110.1:c.686A>G | ENSP00000496392.1:p.Asn229Ser | |
| ENST00000265849.11:c.1004A>G | ENSP00000265849.7:p.Asn335Ser | |
| ENST00000382321.5:c.804-6949A>G | ENSP00000371758.4:n.804-6949A>G | |
| ENST00000406569.7:n.1004A>G | ||
| ENST00000441476.6:c.686A>G | ENSP00000392843.2:p.Asn229Ser | |
| ENST00000469652.1:n.63-7035A>G | ||
| NM_000535.5:c.1004A>G , LRG_161t1:c.1004A>G | NP_000526.1:p.Asn335Ser | |
| NR_003085.2:n.1086A>G | ||
| XM_006715742.2:c.998A>G | XP_006715805.1:p.Asn333Ser | |
| XM_006715744.2:c.71A>G | XP_006715807.1:p.Asn24Ser | |
| XM_011515427.1:c.1049A>G | XP_011513729.1:p.Asn350Ser | |
| XM_011515428.1:c.1033+2033A>G | XP_011513730.1:n.1033+2033A>G | |
| XM_011515429.1:c.686A>G | XP_011513731.1:p.Asn229Ser | |
| XM_011515430.1:c.686A>G | XP_011513732.1:p.Asn229Ser | |
| NM_000535.6:c.1004A>G | NP_000526.2:p.Asn335Ser | |
| NM_001322003.1:c.599A>G | NP_001308932.1:p.Asn200Ser | |
| NM_001322004.1:c.599A>G | NP_001308933.1:p.Asn200Ser | |
| NM_001322005.1:c.599A>G | NP_001308934.1:p.Asn200Ser | |
| NM_001322006.1:c.988+2033A>G | NP_001308935.1:n.988+2033A>G | |
| NM_001322007.1:c.686A>G | NP_001308936.1:p.Asn229Ser | |
| NM_001322008.1:c.686A>G | NP_001308937.1:p.Asn229Ser | |
| NM_001322009.1:c.599A>G | NP_001308938.1:p.Asn200Ser | |
| NM_001322010.1:c.583+2033A>G | NP_001308939.1:n.583+2033A>G | |
| NM_001322011.1:c.71A>G | NP_001308940.1:p.Asn24Ser | |
| NM_001322012.1:c.71A>G | NP_001308941.1:p.Asn24Ser | |
| NM_001322013.1:c.431A>G | NP_001308942.1:p.Asn144Ser | |
| NM_001322014.1:c.1004A>G | NP_001308943.1:p.Asn335Ser | |
| NM_001322015.1:c.695A>G | NP_001308944.1:p.Asn232Ser | |
| NR_136154.1:n.1091A>G | ||
| XM_006715744.4:c.71A>G | XP_006715807.1:p.Asn24Ser | |
| XM_017012342.2:c.71A>G | XP_016867831.1:p.Asn24Ser | |
| XM_024446800.1:c.583+2033A>G | XP_024302568.1:n.583+2033A>G | |
| NM_000535.7:c.1004A>G MANE Select | NP_000526.2:p.Asn335Ser | |
| NM_001322003.2:c.599A>G | NP_001308932.1:p.Asn200Ser | |
| NM_001322004.2:c.599A>G | NP_001308933.1:p.Asn200Ser | |
| NM_001322005.2:c.599A>G | NP_001308934.1:p.Asn200Ser | |
| NM_001322006.2:c.988+2033A>G | NP_001308935.1:n.988+2033A>G | |
| NM_001322008.2:c.686A>G | NP_001308937.1:p.Asn229Ser | |
| NM_001322009.2:c.599A>G | NP_001308938.1:p.Asn200Ser | |
| NM_001322010.2:c.583+2033A>G | NP_001308939.1:n.583+2033A>G | |
| NM_001322011.2:c.71A>G | NP_001308940.1:p.Asn24Ser | |
| NM_001322012.2:c.71A>G | NP_001308941.1:p.Asn24Ser | |
| NM_001322013.2:c.431A>G | NP_001308942.1:p.Asn144Ser | |
| NM_001322014.2:c.1004A>G | NP_001308943.1:p.Asn335Ser | |
| NM_001322015.2:c.695A>G | NP_001308944.1:p.Asn232Ser | |
| NM_001322007.2:c.686A>G | NP_001308936.1:p.Asn229Ser |