HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862336T= , CM000666.2:g.4862336T= | GRCh38 |
NC_000004.11:g.4864063T= , CM000666.1:g.4864063T= | GRCh37 |
NC_000004.10:g.4914964T= | NCBI36 |
NG_008121.1:g.7672T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-365T= MANE Select | ENSP00000372170.4:n.470-365T= | |
ENST00000382723.4:c.470-365T= | ENSP00000372170.4:n.470-365T= | |
NM_002448.3:c.470-365T= MANE Select | NP_002439.2:n.470-365T= |