HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4863026C= , CM000666.2:g.4863026C= | GRCh38 |
NC_000004.11:g.4864753C= , CM000666.1:g.4864753C= | GRCh37 |
NC_000004.10:g.4915654C= | NCBI36 |
NG_008121.1:g.8362C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.795C= MANE Select | ENSP00000372170.4:p.Ala265= | |
ENST00000382723.4:c.795C= | ENSP00000372170.4:p.Ala265= | |
ENST00000468421.1:n.507C= | ||
NM_002448.3:c.795C= MANE Select | NP_002439.2:p.Ala265= |