HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862488A= , CM000666.2:g.4862488A= | GRCh38 |
NC_000004.11:g.4864215A= , CM000666.1:g.4864215A= | GRCh37 |
NC_000004.10:g.4915116A= | NCBI36 |
NG_008121.1:g.7824A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-213A= MANE Select | ENSP00000372170.4:n.470-213A= | |
ENST00000382723.4:c.470-213A= | ENSP00000372170.4:n.470-213A= | |
ENST00000468421.1:n.61A= | ||
NM_002448.3:c.470-213A= MANE Select | NP_002439.2:n.470-213A= |