HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862662T= , CM000666.2:g.4862662T= | GRCh38 |
NC_000004.11:g.4864389T= , CM000666.1:g.4864389T= | GRCh37 |
NC_000004.10:g.4915290T= | NCBI36 |
NG_008121.1:g.7998T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-39T= MANE Select | ENSP00000372170.4:n.470-39T= | |
ENST00000382723.4:c.470-39T= | ENSP00000372170.4:n.470-39T= | |
ENST00000468421.1:n.182-39T= | ||
NM_002448.3:c.470-39T= MANE Select | NP_002439.2:n.470-39T= |