HGVS | Genome Assembly |
---|---|
NC_000005.10:g.154457465G>A , CM000667.2:g.154457465G>A | GRCh38 |
NC_000005.9:g.153837025G>A , CM000667.1:g.153837025G>A | GRCh37 |
NC_000005.8:g.153817218G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297109.11:c.*1437G>A MANE Select | ENSP00000297109.5:n.*1437G>A | |
ENST00000297109.10:c.*1437G>A | ENSP00000297109.5:n.*1437G>A | |
NM_001131062.1:c.*1437G>A | NP_001124534.1:n.*1437G>A | |
NM_001131063.1:c.*1437G>A | NP_001124535.1:n.*1437G>A | |
NM_024632.5:c.*1437G>A | NP_078908.1:n.*1437G>A | |
NR_024084.1:n.2681G>A | ||
NM_024632.6:c.*1437G>A MANE Select | NP_078908.1:n.*1437G>A | |
NM_001131062.2:c.*1437G>A | NP_001124534.1:n.*1437G>A | |
NM_001131063.2:c.*1437G>A | NP_001124535.1:n.*1437G>A | |
NR_024084.2:n.2641G>A |