HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35849605C= , CM000681.2:g.35849605C= | GRCh38 |
NC_000019.9:g.36340507C= , CM000681.1:g.36340507C= | GRCh37 |
NC_000019.8:g.41032347C= | NCBI36 |
NG_013356.2:g.24683G= , LRG_693:g.24683G= | |
NG_051206.1:g.2971C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.657G= MANE Select | ENSP00000368190.4:p.Ala219= | |
ENST00000353632.6:c.657G= | ENSP00000343634.5:p.Ala219= | |
ENST00000378910.9:c.657G= | ENSP00000368190.4:p.Ala219= | |
NM_004646.3:c.657G= , LRG_693t1:c.657G= | NP_004637.1:p.Ala219= | |
NM_004646.4:c.657G= MANE Select | NP_004637.1:p.Ala219= |