HGVS | Genome Assembly |
---|---|
NC_000001.11:g.159886653C>T , CM000663.2:g.159886653C>T | GRCh38 |
NC_000001.10:g.159856443C>T , CM000663.1:g.159856443C>T | GRCh37 |
NC_000001.9:g.158123067C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368099.9:c.625G>A MANE Select | ENSP00000357079.4:p.Ala209Thr | |
ENST00000368099.8:c.625G>A | ENSP00000357079.4:p.Ala209Thr | |
ENST00000426543.6:c.370G>A | ENSP00000403044.2:p.Ala124Thr | |
ENST00000476696.5:c.625G>A | ENSP00000483972.1:p.Ala209Thr | |
ENST00000479940.2:c.370G>A | ENSP00000478944.1:p.Ala124Thr | |
NM_012337.2:c.625G>A | NP_036469.2:p.Ala209Thr | |
NM_012337.3:c.625G>A MANE Select | NP_036469.2:p.Ala209Thr |