HGVS | Genome Assembly |
---|---|
NC_000004.12:g.40354408C>A , CM000666.2:g.40354408C>A | GRCh38 |
NC_000004.11:g.40356425C>A , CM000666.1:g.40356425C>A | GRCh37 |
NC_000004.10:g.40051182C>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000310169.3:c.1328C>A MANE Select | ENSP00000312663.2:p.Ser443Tyr | |
ENST00000310169.2:c.1328C>A | ENSP00000312663.2:p.Ser443Tyr | |
NM_017581.3:c.1328C>A | NP_060051.2:p.Ser443Tyr | |
NM_017581.4:c.1328C>A MANE Select | NP_060051.2:p.Ser443Tyr |