Linked Data
ClinVar Variation Id:
501609
dbSNP Id:
rs752509045
ExAC:
6:51497421 G / A
gnomAD v2:
6-51497421-G-A
gnomAD v4:
6-51632623-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51632623G>A , CM000668.2:g.51632623G>A | GRCh38 |
| NC_000006.11:g.51497421G>A , CM000668.1:g.51497421G>A | GRCh37 |
| NC_000006.10:g.51605380G>A | NCBI36 |
| NG_008753.1:g.460003C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.11607C>T MANE Select | ENSP00000360158.3:p.Ala3869= | |
| ENST00000371117.7:c.11607C>T | ENSP00000360158.3:p.Ala3869= | |
| NM_138694.3:c.11607C>T | NP_619639.3:p.Ala3869= | |
| XM_011514679.1:c.11607C>T | XP_011512981.1:p.Ala3869= | |
| XM_011514680.1:c.11607C>T | XP_011512982.1:p.Ala3869= | |
| XM_011514681.1:c.11478C>T | XP_011512983.1:p.Ala3826= | |
| XM_011514682.1:c.11469C>T | XP_011512984.1:p.Ala3823= | |
| XM_011514683.1:c.10965C>T | XP_011512985.1:p.Ala3655= | |
| XM_011514684.1:c.10896C>T | XP_011512986.1:p.Ala3632= | |
| XM_011514690.1:c.5682C>T | XP_011512992.1:p.Ala1894= | |
| XM_011514691.1:c.5682C>T | XP_011512993.1:p.Ala1894= | |
| XM_011514680.3:c.11607C>T | XP_011512982.1:p.Ala3869= | |
| XM_011514682.3:c.11469C>T | XP_011512984.1:p.Ala3823= | |
| XM_011514683.3:c.10965C>T | XP_011512985.1:p.Ala3655= | |
| XM_011514684.3:c.10896C>T | XP_011512986.1:p.Ala3632= | |
| XM_011514690.3:c.5682C>T | XP_011512992.1:p.Ala1894= | |
| XM_011514691.3:c.5682C>T | XP_011512993.1:p.Ala1894= | |
| XM_017010944.2:c.11607C>T | XP_016866433.1:p.Ala3869= | |
| XM_017010945.2:c.11532C>T | XP_016866434.1:p.Ala3844= | |
| XM_017010946.2:c.11412C>T | XP_016866435.1:p.Ala3804= | |
| XM_017010947.2:c.11343C>T | XP_016866436.1:p.Ala3781= | |
| XM_017010948.2:c.10896C>T | XP_016866437.1:p.Ala3632= | |
| XM_017010949.2:c.9747C>T | XP_016866438.1:p.Ala3249= | |
| NM_138694.4:c.11607C>T MANE Select | NP_619639.3:p.Ala3869= |