Linked Data
ClinVar Variation Id:
94342
ClinVar RCV Id:
RCV000340623
dbSNP Id:
rs398123795
gnomAD v2:
2-71896853-C-T
gnomAD v4:
2-71669723-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71669723C>T , CM000664.2:g.71669723C>T | GRCh38 |
| NC_000002.11:g.71896853C>T , CM000664.1:g.71896853C>T | GRCh37 |
| NC_000002.10:g.71750361C>T | NCBI36 |
| NG_008694.1:g.221101C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698057.1:c.3175C>T | ENSP00000513536.1:p.Gln1059Ter | |
| ENST00000698058.1:c.2392C>T | ENSP00000513537.1:p.Gln798Ter | |
| ENST00000698059.1:c.2500C>T | ENSP00000513538.1:p.Gln834Ter | |
| ENST00000258104.8:c.5644C>T MANE Plus Clinical | ENSP00000258104.3:p.Gln1882Ter | |
| ENST00000410020.8:c.5761C>T MANE Select | ENSP00000386881.3:p.Gln1921Ter | |
| ENST00000258104.7:c.5644C>T | ENSP00000258104.3:p.Gln1882Ter | |
| ENST00000394120.6:c.5647C>T | ENSP00000377678.2:p.Gln1883Ter | |
| ENST00000409366.5:c.5710C>T | ENSP00000386512.1:p.Gln1904Ter | |
| ENST00000409582.7:c.5758C>T | ENSP00000386547.3:p.Gln1920Ter | |
| ENST00000409651.5:c.5740C>T | ENSP00000386683.1:p.Gln1914Ter | |
| ENST00000409744.5:c.5668C>T | ENSP00000386285.1:p.Gln1890Ter | |
| ENST00000409762.5:c.5695C>T | ENSP00000387137.1:p.Gln1899Ter | |
| ENST00000410020.7:c.5761C>T | ENSP00000386881.3:p.Gln1921Ter | |
| ENST00000410041.1:c.5698C>T | ENSP00000386617.1:p.Gln1900Ter | |
| ENST00000413539.6:c.5737C>T | ENSP00000407046.2:p.Gln1913Ter | |
| ENST00000429174.6:c.5707C>T | ENSP00000398305.2:p.Gln1903Ter | |
| ENST00000479049.6:n.2529C>T | ||
| NM_001130455.1:c.5647C>T | NP_001123927.1:p.Gln1883Ter | |
| NM_001130976.1:c.5602C>T | NP_001124448.1:p.Gln1868Ter | |
| NM_001130977.1:c.5665C>T | NP_001124449.1:p.Gln1889Ter | |
| NM_001130978.1:c.5707C>T | NP_001124450.1:p.Gln1903Ter | |
| NM_001130979.1:c.5737C>T | NP_001124451.1:p.Gln1913Ter | |
| NM_001130980.1:c.5695C>T | NP_001124452.1:p.Gln1899Ter | |
| NM_001130981.1:c.5758C>T | NP_001124453.1:p.Gln1920Ter | |
| NM_001130982.1:c.5740C>T | NP_001124454.1:p.Gln1914Ter | |
| NM_001130983.1:c.5710C>T | NP_001124455.1:p.Gln1904Ter | |
| NM_001130984.1:c.5668C>T | NP_001124456.1:p.Gln1890Ter | |
| NM_001130985.1:c.5698C>T | NP_001124457.1:p.Gln1900Ter | |
| NM_001130986.1:c.5605C>T | NP_001124458.1:p.Gln1869Ter | |
| NM_001130987.1:c.5761C>T | NP_001124459.1:p.Gln1921Ter | |
| NM_003494.3:c.5644C>T | NP_003485.1:p.Gln1882Ter | |
| XM_005264584.3:c.5803C>T | XP_005264641.1:p.Gln1935Ter | |
| XM_005264585.3:c.5800C>T | XP_005264642.1:p.Gln1934Ter | |
| XM_005264584.4:c.5803C>T | XP_005264641.1:p.Gln1935Ter | |
| XM_005264585.5:c.5800C>T | XP_005264642.1:p.Gln1934Ter | |
| NM_001130987.2:c.5761C>T MANE Select | NP_001124459.1:p.Gln1921Ter | |
| NM_001130455.2:c.5647C>T | NP_001123927.1:p.Gln1883Ter | |
| NM_001130976.2:c.5602C>T | NP_001124448.1:p.Gln1868Ter | |
| NM_001130977.2:c.5665C>T | NP_001124449.1:p.Gln1889Ter | |
| NM_001130978.2:c.5707C>T | NP_001124450.1:p.Gln1903Ter | |
| NM_001130979.2:c.5737C>T | NP_001124451.1:p.Gln1913Ter | |
| NM_001130980.2:c.5695C>T | NP_001124452.1:p.Gln1899Ter | |
| NM_001130981.2:c.5758C>T | NP_001124453.1:p.Gln1920Ter | |
| NM_001130982.2:c.5740C>T | NP_001124454.1:p.Gln1914Ter | |
| NM_001130983.2:c.5710C>T | NP_001124455.1:p.Gln1904Ter | |
| NM_001130984.2:c.5668C>T | NP_001124456.1:p.Gln1890Ter | |
| NM_001130985.2:c.5698C>T | NP_001124457.1:p.Gln1900Ter | |
| NM_001130986.2:c.5605C>T | NP_001124458.1:p.Gln1869Ter | |
| NM_003494.4:c.5644C>T MANE Plus Clinical | NP_003485.1:p.Gln1882Ter |