Linked Data
ClinVar Variation Id:
43271
ClinVar RCV Id:
RCV000036176
RCV000306975
RCV000366371
RCV000404997
RCV000724217
RCV001272803
RCV004534757
dbSNP Id:
rs199561332
ExAC:
11:76913409 C / T
gnomAD v2:
11-76913409-C-T
gnomAD v3:
11-77202364-C-T
gnomAD v4:
11-77202364-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.77202364C>T , CM000673.2:g.77202364C>T | GRCh38 |
| NC_000011.9:g.76913409C>T , CM000673.1:g.76913409C>T | GRCh37 |
| NC_000011.8:g.76591057C>T | NCBI36 |
| NG_009086.1:g.79100C>T | |
| NG_009086.2:g.79119C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409709.9:c.5108C>T MANE Select | ENSP00000386331.3:p.Ala1703Val | |
| ENST00000670577.1:c.2949C>T | ||
| ENST00000409619.6:c.4961C>T | ENSP00000386635.2:p.Ala1654Val | |
| ENST00000409709.7:c.5108C>T | ENSP00000386331.3:p.Ala1703Val | |
| ENST00000458169.2:c.2534C>T | ENSP00000417017.2:p.Ala845Val | |
| ENST00000458637.6:c.4994C>T | ENSP00000392185.2:p.Ala1665Val | |
| ENST00000481328.7:n.2644C>T | ||
| NM_000260.3:c.5108C>T | NP_000251.3:p.Ala1703Val | |
| NM_001127180.1:c.4994C>T | NP_001120652.1:p.Ala1665Val | |
| XM_005274012.2:c.4991C>T | XP_005274069.1:p.Ala1664Val | |
| XM_006718558.2:c.5099C>T | XP_006718621.1:p.Ala1700Val | |
| XM_006718559.2:c.4994C>T | XP_006718622.1:p.Ala1665Val | |
| XM_006718560.2:c.4991C>T | XP_006718623.1:p.Ala1664Val | |
| XM_006718561.2:c.4994C>T | XP_006718624.1:p.Ala1665Val | |
| XM_011545044.1:c.5108C>T | XP_011543346.1:p.Ala1703Val | |
| XM_011545045.1:c.5102C>T | XP_011543347.1:p.Ala1701Val | |
| XM_011545046.1:c.5075C>T | XP_011543348.1:p.Ala1692Val | |
| XM_011545047.1:c.5012C>T | XP_011543349.1:p.Ala1671Val | |
| XM_011545048.1:c.4883C>T | XP_011543350.1:p.Ala1628Val | |
| XM_011545049.1:c.4871C>T | XP_011543351.1:p.Ala1624Val | |
| XM_011545050.1:c.4844C>T | XP_011543352.1:p.Ala1615Val | |
| XM_011545051.1:c.5108C>T | XP_011543353.1:p.Ala1703Val | |
| XM_011545052.1:c.5108C>T | XP_011543354.1:p.Ala1703Val | |
| XR_949938.1:n.5428C>T | ||
| XR_949941.1:n.5428C>T | ||
| XR_949942.1:n.5430C>T | ||
| XM_011545044.2:c.5108C>T | XP_011543346.1:p.Ala1703Val | |
| XM_011545046.2:c.5198C>T | XP_011543348.2:p.Ala1733Val | |
| XM_011545050.2:c.4844C>T | XP_011543352.1:p.Ala1615Val | |
| XM_017017778.1:c.5192C>T | XP_016873267.1:p.Ala1731Val | |
| XM_017017779.1:c.5189C>T | XP_016873268.1:p.Ala1730Val | |
| XM_017017780.1:c.5198C>T | XP_016873269.1:p.Ala1733Val | |
| XM_017017781.1:c.5102C>T | XP_016873270.1:p.Ala1701Val | |
| XM_017017782.1:c.5084C>T | XP_016873271.1:p.Ala1695Val | |
| XM_017017783.1:c.5081C>T | XP_016873272.1:p.Ala1694Val | |
| XM_017017784.1:c.5081C>T | XP_016873273.1:p.Ala1694Val | |
| XM_017017785.1:c.4961C>T | XP_016873274.1:p.Ala1654Val | |
| XM_017017786.1:c.5198C>T | XP_016873275.1:p.Ala1733Val | |
| XM_017017788.1:c.5084C>T | XP_016873277.1:p.Ala1695Val | |
| XR_001747885.1:n.5213C>T | ||
| XR_001747886.1:n.5213C>T | ||
| XR_001747887.1:n.5213C>T | ||
| XR_001747888.1:n.5213C>T | ||
| NM_000260.4:c.5108C>T MANE Select | NP_000251.3:p.Ala1703Val | |
| NM_001127180.2:c.4994C>T | NP_001120652.1:p.Ala1665Val | |
| NM_001369365.1:c.4961C>T | NP_001356294.1:p.Ala1654Val |