HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65240137T>A , CM000674.2:g.65240137T>A | GRCh38 |
NC_000012.11:g.65633917T>A , CM000674.1:g.65633917T>A | GRCh37 |
NC_000012.10:g.63920184T>A | NCBI36 |
NG_016210.1:g.75567T>A | |
NG_016210.2:g.75567T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.2025T>A MANE Select | ENSP00000308369.2:p.Asp675Glu | |
ENST00000308330.2:c.2025T>A | ENSP00000308369.2:p.Asp675Glu | |
NM_001167614.1:c.2022T>A | NP_001161086.1:p.Asp674Glu | |
NM_014319.4:c.2025T>A | NP_055134.2:p.Asp675Glu | |
NM_014319.5:c.2025T>A MANE Select | NP_055134.2:p.Asp675Glu | |
NM_001167614.2:c.2022T>A | NP_001161086.1:p.Asp674Glu |