HGVS | Genome Assembly |
---|---|
NC_000001.11:g.159886652G>A , CM000663.2:g.159886652G>A | GRCh38 |
NC_000001.10:g.159856442G>A , CM000663.1:g.159856442G>A | GRCh37 |
NC_000001.9:g.158123066G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368099.9:c.626C>T MANE Select | ENSP00000357079.4:p.Ala209Val | |
ENST00000368099.8:c.626C>T | ENSP00000357079.4:p.Ala209Val | |
ENST00000426543.6:c.371C>T | ENSP00000403044.2:p.Ala124Val | |
ENST00000476696.5:c.626C>T | ENSP00000483972.1:p.Ala209Val | |
ENST00000479940.2:c.371C>T | ENSP00000478944.1:p.Ala124Val | |
NM_012337.2:c.626C>T | NP_036469.2:p.Ala209Val | |
NM_012337.3:c.626C>T MANE Select | NP_036469.2:p.Ala209Val |