HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862728T= , CM000666.2:g.4862728T= | GRCh38 |
NC_000004.11:g.4864455T= , CM000666.1:g.4864455T= | GRCh37 |
NC_000004.10:g.4915356T= | NCBI36 |
NG_008121.1:g.8064T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.497T= MANE Select | ENSP00000372170.4:p.Leu166= | |
ENST00000382723.4:c.497T= | ENSP00000372170.4:p.Leu166= | |
ENST00000468421.1:n.209T= | ||
NM_002448.3:c.497T= MANE Select | NP_002439.2:p.Leu166= |