HGVS | Genome Assembly |
---|---|
NC_000001.11:g.159886651G>C , CM000663.2:g.159886651G>C | GRCh38 |
NC_000001.10:g.159856441G>C , CM000663.1:g.159856441G>C | GRCh37 |
NC_000001.9:g.158123065G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368099.9:c.627C>G MANE Select | ENSP00000357079.4:p.Ala209= | |
ENST00000368099.8:c.627C>G | ENSP00000357079.4:p.Ala209= | |
ENST00000426543.6:c.372C>G | ENSP00000403044.2:p.Ala124= | |
ENST00000476696.5:c.627C>G | ENSP00000483972.1:p.Ala209= | |
ENST00000479940.2:c.372C>G | ENSP00000478944.1:p.Ala124= | |
NM_012337.2:c.627C>G | NP_036469.2:p.Ala209= | |
NM_012337.3:c.627C>G MANE Select | NP_036469.2:p.Ala209= |