Linked Data
ClinVar Variation Id:
288630
ClinVar RCV Id:
RCV000310014
RCV000362344
RCV000388999
RCV000493108
RCV001079670
RCV000986770
RCV001526431
dbSNP Id:
rs141137410
ExAC:
2:71891537 G / T
gnomAD v2:
2-71891537-G-T
gnomAD v3:
2-71664407-G-T
gnomAD v4:
2-71664407-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71664407G>T , CM000664.2:g.71664407G>T | GRCh38 |
| NC_000002.11:g.71891537G>T , CM000664.1:g.71891537G>T | GRCh37 |
| NC_000002.10:g.71745045G>T | NCBI36 |
| NG_008694.1:g.215785G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2557G>T | ENSP00000513536.1:p.Ala853Ser | |
| ENST00000698058.1:c.1774G>T | ENSP00000513537.1:p.Ala592Ser | |
| ENST00000698059.1:c.1882G>T | ENSP00000513538.1:p.Ala628Ser | |
| ENST00000258104.8:c.5026G>T MANE Plus Clinical | ENSP00000258104.3:p.Ala1676Ser | |
| ENST00000410020.8:c.5143G>T MANE Select | ENSP00000386881.3:p.Ala1715Ser | |
| ENST00000258104.7:c.5026G>T | ENSP00000258104.3:p.Ala1676Ser | |
| ENST00000394120.6:c.5029G>T | ENSP00000377678.2:p.Ala1677Ser | |
| ENST00000409366.5:c.5092G>T | ENSP00000386512.1:p.Ala1698Ser | |
| ENST00000409582.7:c.5140G>T | ENSP00000386547.3:p.Ala1714Ser | |
| ENST00000409651.5:c.5122G>T | ENSP00000386683.1:p.Ala1708Ser | |
| ENST00000409744.5:c.5050G>T | ENSP00000386285.1:p.Ala1684Ser | |
| ENST00000409762.5:c.5077G>T | ENSP00000387137.1:p.Ala1693Ser | |
| ENST00000410020.7:c.5143G>T | ENSP00000386881.3:p.Ala1715Ser | |
| ENST00000410041.1:c.5080G>T | ENSP00000386617.1:p.Ala1694Ser | |
| ENST00000413539.6:c.5119G>T | ENSP00000407046.2:p.Ala1707Ser | |
| ENST00000429174.6:c.5089G>T | ENSP00000398305.2:p.Ala1697Ser | |
| ENST00000479049.6:n.1911G>T | ||
| NM_001130455.1:c.5029G>T | NP_001123927.1:p.Ala1677Ser | |
| NM_001130976.1:c.4984G>T | NP_001124448.1:p.Ala1662Ser | |
| NM_001130977.1:c.5047G>T | NP_001124449.1:p.Ala1683Ser | |
| NM_001130978.1:c.5089G>T | NP_001124450.1:p.Ala1697Ser | |
| NM_001130979.1:c.5119G>T | NP_001124451.1:p.Ala1707Ser | |
| NM_001130980.1:c.5077G>T | NP_001124452.1:p.Ala1693Ser | |
| NM_001130981.1:c.5140G>T | NP_001124453.1:p.Ala1714Ser | |
| NM_001130982.1:c.5122G>T | NP_001124454.1:p.Ala1708Ser | |
| NM_001130983.1:c.5092G>T | NP_001124455.1:p.Ala1698Ser | |
| NM_001130984.1:c.5050G>T | NP_001124456.1:p.Ala1684Ser | |
| NM_001130985.1:c.5080G>T | NP_001124457.1:p.Ala1694Ser | |
| NM_001130986.1:c.4987G>T | NP_001124458.1:p.Ala1663Ser | |
| NM_001130987.1:c.5143G>T | NP_001124459.1:p.Ala1715Ser | |
| NM_003494.3:c.5026G>T | NP_003485.1:p.Ala1676Ser | |
| XM_005264584.3:c.5185G>T | XP_005264641.1:p.Ala1729Ser | |
| XM_005264585.3:c.5182G>T | XP_005264642.1:p.Ala1728Ser | |
| XM_005264584.4:c.5185G>T | XP_005264641.1:p.Ala1729Ser | |
| XM_005264585.5:c.5182G>T | XP_005264642.1:p.Ala1728Ser | |
| XR_001738969.1:n.5343G>T | ||
| NM_001130987.2:c.5143G>T MANE Select | NP_001124459.1:p.Ala1715Ser | |
| NM_001130455.2:c.5029G>T | NP_001123927.1:p.Ala1677Ser | |
| NM_001130976.2:c.4984G>T | NP_001124448.1:p.Ala1662Ser | |
| NM_001130977.2:c.5047G>T | NP_001124449.1:p.Ala1683Ser | |
| NM_001130978.2:c.5089G>T | NP_001124450.1:p.Ala1697Ser | |
| NM_001130979.2:c.5119G>T | NP_001124451.1:p.Ala1707Ser | |
| NM_001130980.2:c.5077G>T | NP_001124452.1:p.Ala1693Ser | |
| NM_001130981.2:c.5140G>T | NP_001124453.1:p.Ala1714Ser | |
| NM_001130982.2:c.5122G>T | NP_001124454.1:p.Ala1708Ser | |
| NM_001130983.2:c.5092G>T | NP_001124455.1:p.Ala1698Ser | |
| NM_001130984.2:c.5050G>T | NP_001124456.1:p.Ala1684Ser | |
| NM_001130985.2:c.5080G>T | NP_001124457.1:p.Ala1694Ser | |
| NM_001130986.2:c.4987G>T | NP_001124458.1:p.Ala1663Ser | |
| NM_003494.4:c.5026G>T MANE Plus Clinical | NP_003485.1:p.Ala1676Ser |