HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862572G>T , CM000666.2:g.4862572G>T | GRCh38 |
NC_000004.11:g.4864299G>T , CM000666.1:g.4864299G>T | GRCh37 |
NC_000004.10:g.4915200G>T | NCBI36 |
NG_008121.1:g.7908G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-129G>T MANE Select | ENSP00000372170.4:n.470-129G>T | |
ENST00000382723.4:c.470-129G>T | ENSP00000372170.4:n.470-129G>T | |
ENST00000468421.1:n.145G>T | ||
NM_002448.3:c.470-129G>T MANE Select | NP_002439.2:n.470-129G>T |