HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204159524G= , CM000663.2:g.204159524G= | GRCh38 |
NC_000001.10:g.204128652G= , CM000663.1:g.204128652G= | GRCh37 |
NC_000001.9:g.202395275G= | NCBI36 |
NG_012122.1:g.11814C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272190.9:c.564C= MANE Select | ENSP00000272190.8:p.Ala188= | |
ENST00000638118.1:c.450C= | ENSP00000490307.1:p.Ala150= | |
ENST00000272190.8:c.564C= | ENSP00000272190.8:p.Ala188= | |
NM_000537.3:c.564C= | NP_000528.1:p.Ala188= | |
NM_000537.4:c.564C= MANE Select | NP_000528.1:p.Ala188= |