HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20759874C>G , CM000686.2:g.20759874C>G | GRCh38 |
NC_000024.9:g.22921760C>G , CM000686.1:g.22921760C>G | GRCh37 |
NC_000024.8:g.21331148C>G | NCBI36 |
NG_032924.1:g.8807C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000629237.2:c.88C>G MANE Select | ENSP00000486252.1:p.Arg30Gly | |
ENST00000629237.1:c.88C>G | ENSP00000486252.1:p.Arg30Gly | |
NM_001039567.2:c.88C>G | NP_001034656.1:p.Arg30Gly | |
XM_011531423.1:c.37C>G | XP_011529725.1:p.Arg13Gly | |
NM_001039567.3:c.88C>G MANE Select | NP_001034656.1:p.Arg30Gly |