HGVS | Genome Assembly |
---|---|
NC_000003.12:g.173019503C>A , CM000665.2:g.173019503C>A | GRCh38 |
NC_000003.11:g.172737293C>A , CM000665.1:g.172737293C>A | GRCh37 |
NC_000003.10:g.174219987C>A | NCBI36 |
NG_021422.1:g.126766G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351008.4:c.831G>T MANE Select | ENSP00000341765.3:p.Arg277Ser | |
ENST00000351008.3:c.831G>T | ENSP00000341765.3:p.Arg277Ser | |
NM_031955.5:c.831G>T | NP_114161.3:p.Arg277Ser | |
XM_006713778.2:c.831G>T | XP_006713841.1:p.Arg277Ser | |
XM_011513222.1:c.831G>T | XP_011511524.1:p.Arg277Ser | |
XM_006713778.3:c.831G>T | XP_006713841.1:p.Arg277Ser | |
XM_017007308.2:c.831G>T | XP_016862797.1:p.Arg277Ser | |
NM_031955.6:c.831G>T MANE Select | NP_114161.3:p.Arg277Ser |