HGVS | Genome Assembly |
---|---|
NC_000003.12:g.173080976G= , CM000665.2:g.173080976G= | GRCh38 |
NC_000003.11:g.172798766G= , CM000665.1:g.172798766G= | GRCh37 |
NC_000003.10:g.174281460G= | NCBI36 |
NG_021422.1:g.65293C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351008.4:c.613-31882C= MANE Select | ENSP00000341765.3:n.613-31882C= | |
ENST00000351008.3:c.613-31882C= | ENSP00000341765.3:n.613-31882C= | |
NM_031955.5:c.613-31882C= | NP_114161.3:n.613-31882C= | |
XM_006713778.2:c.613-31882C= | XP_006713841.1:n.613-31882C= | |
XM_011513222.1:c.613-31882C= | XP_011511524.1:n.613-31882C= | |
XM_006713778.3:c.613-31882C= | XP_006713841.1:n.613-31882C= | |
XM_017007308.2:c.613-31882C= | XP_016862797.1:n.613-31882C= | |
NM_031955.6:c.613-31882C= MANE Select | NP_114161.3:n.613-31882C= |