Linked Data
ClinVar Variation Id:
360540
ClinVar RCV Id:
RCV000305442
dbSNP Id:
rs148520351
ExAC:
7:6012923 T / C
gnomAD v2:
7-6012923-T-C
gnomAD v3:
7-5973292-T-C
gnomAD v4:
7-5973292-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5973292T>C , CM000669.2:g.5973292T>C | GRCh38 |
| NC_000007.13:g.6012923T>C , CM000669.1:g.6012923T>C | GRCh37 |
| NC_000007.12:g.5979449T>C | NCBI36 |
| NG_008466.1:g.40815A>G , LRG_161:g.40815A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*2092A>G | ENSP00000514615.2:n.*2092A>G | |
| ENST00000699840.2:c.*107A>G | ENSP00000514638.2:n.*107A>G | |
| ENST00000699930.2:c.*107A>G | ENSP00000514695.2:n.*107A>G | |
| ENST00000406569.8:c.2056A>G | ENSP00000514464.1:n.2056A>G | |
| ENST00000699752.1:c.*107A>G | ENSP00000514561.1:n.*107A>G | |
| ENST00000699753.1:c.*2117A>G | ENSP00000514562.1:n.*2117A>G | |
| ENST00000699754.1:c.*107A>G | ENSP00000514563.1:n.*107A>G | |
| ENST00000699755.1:c.*2095A>G | ENSP00000514564.1:n.*2095A>G | |
| ENST00000699756.1:c.*2283A>G | ENSP00000514565.1:n.*2283A>G | |
| ENST00000699757.1:c.*1953A>G | ENSP00000514566.1:n.*1953A>G | |
| ENST00000699758.1:c.*1953A>G | ENSP00000514567.1:n.*1953A>G | |
| ENST00000699759.1:n.3550A>G | ||
| ENST00000699760.1:c.*107A>G | ENSP00000514568.1:n.*107A>G | |
| ENST00000699761.1:c.*107A>G | ENSP00000514569.1:n.*107A>G | |
| ENST00000699762.1:c.*107A>G | ENSP00000514570.1:n.*107A>G | |
| ENST00000699763.1:c.*1786A>G | ENSP00000514571.1:n.*1786A>G | |
| ENST00000699764.1:c.*1014A>G | ENSP00000514572.1:n.*1014A>G | |
| ENST00000699765.1:c.*1691A>G | ENSP00000514573.1:n.*1691A>G | |
| ENST00000699766.1:c.*107A>G | ENSP00000514574.1:n.*107A>G | |
| ENST00000699767.1:c.*337A>G | ENSP00000514575.1:n.*337A>G | |
| ENST00000699768.1:c.*107A>G | ENSP00000514576.1:n.*107A>G | |
| ENST00000699811.1:c.*107A>G | ENSP00000514614.1:n.*107A>G | |
| ENST00000699813.1:n.2809A>G | ||
| ENST00000699814.1:c.2319A>G | ||
| ENST00000699815.1:c.*2227A>G | ENSP00000514616.1:n.*2227A>G | |
| ENST00000699816.1:c.*1586A>G | ENSP00000514617.1:n.*1586A>G | |
| ENST00000699817.1:c.*2290A>G | ENSP00000514618.1:n.*2290A>G | |
| ENST00000699818.1:c.*107A>G | ENSP00000514619.1:n.*107A>G | |
| ENST00000699819.1:c.*1853A>G | ENSP00000514620.1:n.*1853A>G | |
| ENST00000699820.1:c.*634A>G | ENSP00000514621.1:n.*634A>G | |
| ENST00000699821.1:c.*107A>G | ENSP00000514622.1:n.*107A>G | |
| ENST00000699822.1:c.*2148A>G | ENSP00000514623.1:n.*2148A>G | |
| ENST00000699823.1:c.*107A>G | ENSP00000514624.1:n.*107A>G | |
| ENST00000699824.1:c.*2199A>G | ENSP00000514625.1:n.*2199A>G | |
| ENST00000699825.1:c.*107A>G | ENSP00000514626.1:n.*107A>G | |
| ENST00000699826.1:c.*2095A>G | ENSP00000514627.1:n.*2095A>G | |
| ENST00000699827.1:c.*107A>G | ENSP00000514628.1:n.*107A>G | |
| ENST00000699828.1:c.*1786A>G | ENSP00000514629.1:n.*1786A>G | |
| ENST00000699833.1:n.4468A>G | ||
| ENST00000699837.1:c.*107A>G | ENSP00000514635.1:n.*107A>G | |
| ENST00000699838.1:c.*2596A>G | ENSP00000514636.1:n.*2596A>G | |
| ENST00000699839.1:c.*107A>G | ENSP00000514637.1:n.*107A>G | |
| ENST00000699916.1:c.*1953A>G | ENSP00000514684.1:n.*1953A>G | |
| ENST00000699917.1:c.*2145A>G | ENSP00000514685.1:n.*2145A>G | |
| ENST00000699918.1:c.*2197A>G | ENSP00000514686.1:n.*2197A>G | |
| ENST00000699919.1:c.*2283A>G | ENSP00000514687.1:n.*2283A>G | |
| ENST00000699920.1:c.*2332A>G | ENSP00000514688.1:n.*2332A>G | |
| ENST00000699928.1:c.*634A>G | ENSP00000514693.1:n.*634A>G | |
| ENST00000699951.1:c.*1749A>G | ENSP00000514706.1:n.*1749A>G | |
| ENST00000699952.1:c.*250A>G | ENSP00000514707.1:n.*250A>G | |
| ENST00000265849.12:c.*107A>G MANE Select | ENSP00000265849.7:n.*107A>G | |
| ENST00000642292.1:c.*107A>G | ENSP00000495524.1:n.*107A>G | |
| ENST00000642456.1:c.*107A>G | ENSP00000493814.1:n.*107A>G | |
| ENST00000265849.11:c.*107A>G | ENSP00000265849.7:n.*107A>G | |
| ENST00000441476.6:c.*107A>G | ENSP00000392843.2:n.*107A>G | |
| NM_000535.5:c.*107A>G , LRG_161t1:c.*107A>G | NP_000526.1:n.*107A>G | |
| NR_003085.2:n.2778A>G | ||
| XM_006715742.2:c.*107A>G | XP_006715805.1:n.*107A>G | |
| XM_006715744.2:c.*107A>G | XP_006715807.1:n.*107A>G | |
| XM_011515427.1:c.*107A>G | XP_011513729.1:n.*107A>G | |
| XM_011515428.1:c.*107A>G | XP_011513730.1:n.*107A>G | |
| XM_011515429.1:c.*107A>G | XP_011513731.1:n.*107A>G | |
| XM_011515430.1:c.*107A>G | XP_011513732.1:n.*107A>G | |
| NM_000535.6:c.*107A>G | NP_000526.2:n.*107A>G | |
| NM_001322003.1:c.*107A>G | NP_001308932.1:n.*107A>G | |
| NM_001322004.1:c.*107A>G | NP_001308933.1:n.*107A>G | |
| NM_001322005.1:c.*107A>G | NP_001308934.1:n.*107A>G | |
| NM_001322006.1:c.*107A>G | NP_001308935.1:n.*107A>G | |
| NM_001322007.1:c.*107A>G | NP_001308936.1:n.*107A>G | |
| NM_001322008.1:c.*107A>G | NP_001308937.1:n.*107A>G | |
| NM_001322009.1:c.*107A>G | NP_001308938.1:n.*107A>G | |
| NM_001322010.1:c.*107A>G | NP_001308939.1:n.*107A>G | |
| NM_001322011.1:c.*107A>G | NP_001308940.1:n.*107A>G | |
| NM_001322012.1:c.*107A>G | NP_001308941.1:n.*107A>G | |
| NM_001322013.1:c.*107A>G | NP_001308942.1:n.*107A>G | |
| NM_001322014.1:c.*107A>G | NP_001308943.1:n.*107A>G | |
| NM_001322015.1:c.*107A>G | NP_001308944.1:n.*107A>G | |
| NR_136154.1:n.2740A>G | ||
| XM_006715744.4:c.*107A>G | XP_006715807.1:n.*107A>G | |
| XM_017012342.2:c.*107A>G | XP_016867831.1:n.*107A>G | |
| XM_024446800.1:c.*107A>G | XP_024302568.1:n.*107A>G | |
| NM_000535.7:c.*107A>G MANE Select | NP_000526.2:n.*107A>G | |
| NM_001322003.2:c.*107A>G | NP_001308932.1:n.*107A>G | |
| NM_001322004.2:c.*107A>G | NP_001308933.1:n.*107A>G | |
| NM_001322005.2:c.*107A>G | NP_001308934.1:n.*107A>G | |
| NM_001322006.2:c.*107A>G | NP_001308935.1:n.*107A>G | |
| NM_001322008.2:c.*107A>G | NP_001308937.1:n.*107A>G | |
| NM_001322009.2:c.*107A>G | NP_001308938.1:n.*107A>G | |
| NM_001322010.2:c.*107A>G | NP_001308939.1:n.*107A>G | |
| NM_001322011.2:c.*107A>G | NP_001308940.1:n.*107A>G | |
| NM_001322012.2:c.*107A>G | NP_001308941.1:n.*107A>G | |
| NM_001322013.2:c.*107A>G | NP_001308942.1:n.*107A>G | |
| NM_001322014.2:c.*107A>G | NP_001308943.1:n.*107A>G | |
| NM_001322015.2:c.*107A>G | NP_001308944.1:n.*107A>G | |
| NM_001322007.2:c.*107A>G | NP_001308936.1:n.*107A>G |