Linked Data
ClinVar Variation Id:
178495
ClinVar RCV Id:
RCV000155243
RCV000225571
RCV000411148
RCV000844723
RCV001544789
RCV001831964
RCV004528890
dbSNP Id:
rs376764423
ExAC:
11:76919517 C / T
gnomAD v2:
11-76919517-C-T
gnomAD v3:
11-77208472-C-T
gnomAD v4:
11-77208472-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.77208472C>T , CM000673.2:g.77208472C>T | GRCh38 |
| NC_000011.9:g.76919517C>T , CM000673.1:g.76919517C>T | GRCh37 |
| NC_000011.8:g.76597165C>T | NCBI36 |
| NG_009086.1:g.85208C>T | |
| NG_009086.2:g.85227C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409709.9:c.5899C>T MANE Select | ENSP00000386331.3:p.Arg1967Ter | |
| ENST00000670577.1:c.3726C>T | ||
| ENST00000409619.6:c.5752C>T | ENSP00000386635.2:p.Arg1918Ter | |
| ENST00000409709.7:c.5899C>T | ENSP00000386331.3:p.Arg1967Ter | |
| ENST00000458169.2:c.3325C>T | ENSP00000417017.2:p.Arg1109Ter | |
| ENST00000458637.6:c.5785C>T | ENSP00000392185.2:p.Arg1929Ter | |
| ENST00000481328.7:n.3435C>T | ||
| ENST00000605744.1:n.813C>T | ||
| NM_000260.3:c.5899C>T | NP_000251.3:p.Arg1967Ter | |
| NM_001127180.1:c.5785C>T | NP_001120652.1:p.Arg1929Ter | |
| XM_005274012.2:c.5782C>T | XP_005274069.1:p.Arg1928Ter | |
| XM_006718558.2:c.5890C>T | XP_006718621.1:p.Arg1964Ter | |
| XM_006718559.2:c.5785C>T | XP_006718622.1:p.Arg1929Ter | |
| XM_006718560.2:c.5782C>T | XP_006718623.1:p.Arg1928Ter | |
| XM_006718561.2:c.5785C>T | XP_006718624.1:p.Arg1929Ter | |
| XM_011545044.1:c.5899C>T | XP_011543346.1:p.Arg1967Ter | |
| XM_011545045.1:c.5893C>T | XP_011543347.1:p.Arg1965Ter | |
| XM_011545046.1:c.5866C>T | XP_011543348.1:p.Arg1956Ter | |
| XM_011545047.1:c.5803C>T | XP_011543349.1:p.Arg1935Ter | |
| XM_011545048.1:c.5674C>T | XP_011543350.1:p.Arg1892Ter | |
| XM_011545049.1:c.5662C>T | XP_011543351.1:p.Arg1888Ter | |
| XM_011545050.1:c.5635C>T | XP_011543352.1:p.Arg1879Ter | |
| XM_011545051.1:c.5899C>T | XP_011543353.1:p.Arg1967Ter | |
| XR_949938.1:n.6219C>T | ||
| XR_949941.1:n.6219C>T | ||
| XM_011545044.2:c.5899C>T | XP_011543346.1:p.Arg1967Ter | |
| XM_011545046.2:c.5989C>T | XP_011543348.2:p.Arg1997Ter | |
| XM_011545050.2:c.5635C>T | XP_011543352.1:p.Arg1879Ter | |
| XM_017017778.1:c.5983C>T | XP_016873267.1:p.Arg1995Ter | |
| XM_017017779.1:c.5980C>T | XP_016873268.1:p.Arg1994Ter | |
| XM_017017780.1:c.5989C>T | XP_016873269.1:p.Arg1997Ter | |
| XM_017017781.1:c.5893C>T | XP_016873270.1:p.Arg1965Ter | |
| XM_017017782.1:c.5875C>T | XP_016873271.1:p.Arg1959Ter | |
| XM_017017783.1:c.5872C>T | XP_016873272.1:p.Arg1958Ter | |
| XM_017017784.1:c.5872C>T | XP_016873273.1:p.Arg1958Ter | |
| XM_017017785.1:c.5752C>T | XP_016873274.1:p.Arg1918Ter | |
| XM_017017786.1:c.5989C>T | XP_016873275.1:p.Arg1997Ter | |
| XM_017017788.1:c.5875C>T | XP_016873277.1:p.Arg1959Ter | |
| XR_001747885.1:n.6004C>T | ||
| XR_001747886.1:n.5919C>T | ||
| XR_001747887.1:n.5990C>T | ||
| NM_000260.4:c.5899C>T MANE Select | NP_000251.3:p.Arg1967Ter | |
| NM_001127180.2:c.5785C>T | NP_001120652.1:p.Arg1929Ter | |
| NM_001369365.1:c.5752C>T | NP_001356294.1:p.Arg1918Ter |