Linked Data
ClinVar Variation Id:
385645
ClinVar RCV Id:
RCV000432151
dbSNP Id:
rs776331800
ExAC:
12:2162702 T / G
gnomAD v2:
12-2162702-T-G
gnomAD v4:
12-2053536-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.2053536T>G , CM000674.2:g.2053536T>G | GRCh38 |
| NC_000012.11:g.2162702T>G , CM000674.1:g.2162702T>G | GRCh37 |
| NC_000012.10:g.2032963T>G | NCBI36 |
| NG_008801.2:g.87751T>G , LRG_334:g.87751T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335762.10:c.-27T>G | ENSP00000336982.5:n.-27T>G | |
| ENST00000399617.6:c.-27T>G | ENSP00000382526.1:n.-27T>G | |
| ENST00000399634.6:c.-27T>G | ENSP00000382542.2:n.-27T>G | |
| ENST00000406454.8:c.-27T>G | ENSP00000385896.3:n.-27T>G | |
| ENST00000673589.2:n.252T>G | ||
| ENST00000682462.1:c.140-61688T>G | ENSP00000507105.1:n.140-61688T>G | |
| ENST00000682544.1:c.140-61688T>G | ENSP00000507184.1:n.140-61688T>G | |
| ENST00000682835.1:c.-27T>G | ENSP00000507282.1:n.-27T>G | |
| ENST00000682867.1:n.55+4282T>G | ||
| ENST00000683482.1:c.-27T>G | ENSP00000507169.1:n.-27T>G | |
| ENST00000683781.1:c.140-61688T>G | ENSP00000507434.1:n.140-61688T>G | |
| ENST00000683824.1:c.140-61688T>G | ENSP00000507867.1:n.140-61688T>G | |
| ENST00000683840.1:c.140-61688T>G | ENSP00000507612.1:n.140-61688T>G | |
| ENST00000683956.1:c.140-61688T>G | ENSP00000506882.1:n.140-61688T>G | |
| ENST00000327702.12:c.-27T>G | ENSP00000329877.7:n.-27T>G | |
| ENST00000347598.9:c.-27T>G | ENSP00000266376.6:n.-27T>G | |
| ENST00000399603.6:c.-27T>G MANE Plus Clinical | ENSP00000382512.1:n.-27T>G | |
| ENST00000399641.6:c.-27T>G | ENSP00000382549.1:n.-27T>G | |
| ENST00000399655.6:c.-27T>G MANE Select | ENSP00000382563.1:n.-27T>G | |
| ENST00000672806.1:c.-27T>G | ENSP00000500218.1:n.-27T>G | |
| ENST00000673589.1:n.211T>G | ||
| ENST00000335762.9:c.-27T>G | ENSP00000336982.5:n.-27T>G | |
| ENST00000399655.5:c.-27T>G | ENSP00000382563.1:n.-27T>G | |
| ENST00000543114.1:c.140-61688T>G | ENSP00000445849.1:n.140-61688T>G | |
| NM_000719.6:c.-27T>G , LRG_334t1:c.-27T>G | NP_000710.5:n.-27T>G | |
| NM_001129827.1:c.-27T>G , LRG_334t2:c.-27T>G | NP_001123299.1:n.-27T>G | |
| NM_001129829.1:c.-27T>G | NP_001123301.1:n.-27T>G | |
| NM_001129830.2:c.-27T>G | NP_001123302.2:n.-27T>G | |
| NM_001129831.1:c.-27T>G | NP_001123303.1:n.-27T>G | |
| NM_001129832.1:c.-27T>G | NP_001123304.1:n.-27T>G | |
| NM_001129833.1:c.-27T>G | NP_001123305.1:n.-27T>G | |
| NM_001129834.1:c.-27T>G | NP_001123306.1:n.-27T>G | |
| NM_001129835.1:c.-27T>G | NP_001123307.1:n.-27T>G | |
| NM_001129836.1:c.-27T>G | NP_001123308.1:n.-27T>G | |
| NM_001129837.1:c.-27T>G | NP_001123309.1:n.-27T>G | |
| NM_001129838.1:c.-27T>G | NP_001123310.1:n.-27T>G | |
| NM_001129839.1:c.-27T>G | NP_001123311.1:n.-27T>G | |
| NM_001129840.1:c.-27T>G , LRG_334t4:c.-27T>G | NP_001123312.1:n.-27T>G | |
| NM_001129841.1:c.-27T>G | NP_001123313.1:n.-27T>G | |
| NM_001129842.1:c.-27T>G | NP_001123314.1:n.-27T>G | |
| NM_001129843.1:c.-27T>G | NP_001123315.1:n.-27T>G | |
| NM_001129844.1:c.-27T>G | NP_001123316.1:n.-27T>G | |
| NM_001129846.1:c.-27T>G | NP_001123318.1:n.-27T>G | |
| NM_001167623.1:c.-27T>G | NP_001161095.1:n.-27T>G | |
| NM_001167624.2:c.-27T>G | NP_001161096.2:n.-27T>G | |
| NM_001167625.1:c.-27T>G | NP_001161097.1:n.-27T>G | |
| NM_199460.3:c.-27T>G | NP_955630.3:n.-27T>G | |
| XM_006719017.1:c.140-61688T>G | XP_006719080.1:n.140-61688T>G | |
| XM_011521020.1:c.140-61688T>G | XP_011519322.1:n.140-61688T>G | |
| XM_011521021.1:c.-27T>G | XP_011519323.1:n.-27T>G | |
| XM_011521022.1:c.-27T>G | XP_011519324.1:n.-27T>G | |
| XM_011521023.1:c.-27T>G | XP_011519325.1:n.-27T>G | |
| XM_006719017.2:c.140-61688T>G | XP_006719080.1:n.140-61688T>G | |
| XM_011521020.2:c.140-61688T>G | XP_011519322.1:n.140-61688T>G | |
| XM_011521023.3:c.-27T>G | XP_011519325.1:n.-27T>G | |
| XM_017019926.2:c.217+17947T>G | XP_016875415.1:n.217+17947T>G | |
| XM_017019927.2:c.217+17947T>G | XP_016875416.1:n.217+17947T>G | |
| XM_017019928.2:c.217+17947T>G | XP_016875417.1:n.217+17947T>G | |
| XM_017019929.2:c.217+17947T>G | XP_016875418.1:n.217+17947T>G | |
| XM_017019930.2:c.217+17947T>G | XP_016875419.1:n.217+17947T>G | |
| XM_017019931.2:c.217+17947T>G | XP_016875420.1:n.217+17947T>G | |
| XM_017019932.2:c.217+17947T>G | XP_016875421.1:n.217+17947T>G | |
| XM_017019933.2:c.217+17947T>G | XP_016875422.1:n.217+17947T>G | |
| XM_017019934.2:c.217+17947T>G | XP_016875423.1:n.217+17947T>G | |
| XM_017019935.2:c.217+17947T>G | XP_016875424.1:n.217+17947T>G | |
| XM_017019936.2:c.217+17947T>G | XP_016875425.1:n.217+17947T>G | |
| XM_017019937.2:c.217+17947T>G | XP_016875426.1:n.217+17947T>G | |
| XM_017019938.2:c.217+17947T>G | XP_016875427.1:n.217+17947T>G | |
| XM_017019939.2:c.217+17947T>G | XP_016875428.1:n.217+17947T>G | |
| XM_017019940.2:c.217+17947T>G | XP_016875429.1:n.217+17947T>G | |
| XM_017019941.2:c.217+17947T>G | XP_016875430.1:n.217+17947T>G | |
| XM_017019942.2:c.217+17947T>G | XP_016875431.1:n.217+17947T>G | |
| XM_017019943.2:c.217+17947T>G | XP_016875432.1:n.217+17947T>G | |
| XM_017019944.2:c.217+17947T>G | XP_016875433.1:n.217+17947T>G | |
| XM_017019945.2:c.217+17947T>G | XP_016875434.1:n.217+17947T>G | |
| XM_017019946.2:c.217+17947T>G | XP_016875435.1:n.217+17947T>G | |
| XM_017019947.2:c.217+17947T>G | XP_016875436.1:n.217+17947T>G | |
| XM_017019948.2:c.217+17947T>G | XP_016875437.1:n.217+17947T>G | |
| XM_017019949.2:c.217+17947T>G | XP_016875438.1:n.217+17947T>G | |
| XM_017019950.2:c.217+17947T>G | XP_016875439.1:n.217+17947T>G | |
| XM_017019951.2:c.217+17947T>G | XP_016875440.1:n.217+17947T>G | |
| XM_017019952.2:c.217+17947T>G | XP_016875441.1:n.217+17947T>G | |
| XM_017019953.1:c.140-61688T>G | XP_016875442.1:n.140-61688T>G | |
| XM_017019954.1:c.140-61688T>G | XP_016875443.1:n.140-61688T>G | |
| XM_017019955.2:c.217+17947T>G | XP_016875444.1:n.217+17947T>G | |
| NM_000719.7:c.-27T>G MANE Select | NP_000710.5:n.-27T>G | |
| NM_001129827.2:c.-27T>G | NP_001123299.1:n.-27T>G | |
| NM_001129830.3:c.-27T>G | NP_001123302.2:n.-27T>G | |
| NM_001129840.2:c.-27T>G | NP_001123312.1:n.-27T>G | |
| NM_001167623.2:c.-27T>G MANE Plus Clinical | NP_001161095.1:n.-27T>G | |
| NM_001129829.2:c.-27T>G | NP_001123301.1:n.-27T>G | |
| NM_001129831.2:c.-27T>G | NP_001123303.1:n.-27T>G | |
| NM_001129832.2:c.-27T>G | NP_001123304.1:n.-27T>G | |
| NM_001129833.2:c.-27T>G | NP_001123305.1:n.-27T>G | |
| NM_001129834.2:c.-27T>G | NP_001123306.1:n.-27T>G | |
| NM_001129835.2:c.-27T>G | NP_001123307.1:n.-27T>G | |
| NM_001129836.2:c.-27T>G | NP_001123308.1:n.-27T>G | |
| NM_001129837.2:c.-27T>G | NP_001123309.1:n.-27T>G | |
| NM_001129838.2:c.-27T>G | NP_001123310.1:n.-27T>G | |
| NM_001129839.2:c.-27T>G | NP_001123311.1:n.-27T>G | |
| NM_001129841.2:c.-27T>G | NP_001123313.1:n.-27T>G | |
| NM_001129842.2:c.-27T>G | NP_001123314.1:n.-27T>G | |
| NM_001129843.2:c.-27T>G | NP_001123315.1:n.-27T>G | |
| NM_001129844.2:c.-27T>G | NP_001123316.1:n.-27T>G | |
| NM_001129846.2:c.-27T>G | NP_001123318.1:n.-27T>G | |
| NM_001167624.3:c.-27T>G | NP_001161096.2:n.-27T>G | |
| NM_001167625.2:c.-27T>G | NP_001161097.1:n.-27T>G | |
| NM_199460.4:c.-27T>G | NP_955630.3:n.-27T>G |