HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31637422G>A , CM000668.2:g.31637422G>A | GRCh38 |
NC_000006.11:g.31605199G>A , CM000668.1:g.31605199G>A | GRCh37 |
NC_000006.10:g.31713178G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376033.3:c.6334-24G>A MANE Select | ENSP00000365201.2:n.6334-24G>A | |
ENST00000376007.8:c.6334-24G>A | ENSP00000365175.4:n.6334-24G>A | |
ENST00000376033.2:c.6334-24G>A | ENSP00000365201.2:n.6334-24G>A | |
ENST00000462617.1:n.666G>A | ||
ENST00000482441.1:n.394-24G>A | ||
ENST00000492691.5:n.769G>A | ||
NM_004638.3:c.6334-24G>A | NP_004629.3:n.6334-24G>A | |
NM_080686.2:c.6334-24G>A | NP_542417.2:n.6334-24G>A | |
XM_011514890.1:c.6121-24G>A | XP_011513192.1:n.6121-24G>A | |
XM_017011274.1:c.6121-24G>A | XP_016866763.1:n.6121-24G>A | |
NM_004638.4:c.6334-24G>A MANE Select | NP_004629.3:n.6334-24G>A | |
NM_080686.3:c.6334-24G>A | NP_542417.2:n.6334-24G>A |