HGVS | Genome Assembly |
---|---|
NC_000003.12:g.173019412T>C , CM000665.2:g.173019412T>C | GRCh38 |
NC_000003.11:g.172737202T>C , CM000665.1:g.172737202T>C | GRCh37 |
NC_000003.10:g.174219896T>C | NCBI36 |
NG_021422.1:g.126857A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351008.4:c.848+74A>G MANE Select | ENSP00000341765.3:n.848+74A>G | |
ENST00000351008.3:c.848+74A>G | ENSP00000341765.3:n.848+74A>G | |
NM_031955.5:c.848+74A>G | NP_114161.3:n.848+74A>G | |
XM_006713778.2:c.848+74A>G | XP_006713841.1:n.848+74A>G | |
XM_011513222.1:c.848+74A>G | XP_011511524.1:n.848+74A>G | |
XM_006713778.3:c.848+74A>G | XP_006713841.1:n.848+74A>G | |
XM_017007308.2:c.848+74A>G | XP_016862797.1:n.848+74A>G | |
NM_031955.6:c.848+74A>G MANE Select | NP_114161.3:n.848+74A>G |