HGVS | Genome Assembly |
---|---|
NC_000004.12:g.119320779T>G , CM000666.2:g.119320779T>G | GRCh38 |
NC_000004.11:g.120241934T>G , CM000666.1:g.120241934T>G | GRCh37 |
NC_000004.10:g.120461382T>G | NCBI36 |
NG_011444.1:g.6383A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274024.4:c.131A>C MANE Select | ENSP00000274024.3:p.Glu44Ala | |
ENST00000274024.3:c.131A>C | ENSP00000274024.3:p.Glu44Ala | |
NM_000134.3:c.131A>C | NP_000125.2:p.Glu44Ala | |
NM_000134.4:c.131A>C MANE Select | NP_000125.2:p.Glu44Ala |