HGVS | Genome Assembly |
---|---|
NC_000020.11:g.32849801G>A , CM000682.2:g.32849801G>A | GRCh38 |
NC_000020.10:g.31437607G>A , CM000682.1:g.31437607G>A | GRCh37 |
NC_000020.9:g.30901268G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375571.6:c.*1073G>A MANE Select | ENSP00000364721.5:n.*1073G>A | |
ENST00000375571.5:c.*1073G>A | ENSP00000364721.5:n.*1073G>A | |
NM_012325.2:c.*1073G>A | NP_036457.1:n.*1073G>A | |
XM_011528696.1:c.*1073G>A | XP_011526998.1:n.*1073G>A | |
XM_011528696.2:c.*1073G>A | XP_011526998.1:n.*1073G>A | |
NM_012325.3:c.*1073G>A MANE Select | NP_036457.1:n.*1073G>A |