HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178515C>T , CM000673.2:g.89178515C>T | GRCh38 |
NC_000011.9:g.88911683C>T , CM000673.1:g.88911683C>T | GRCh37 |
NC_000011.8:g.88551331C>T | NCBI36 |
NG_008748.1:g.5644C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.562C>T MANE Select | ENSP00000263321.4:p.Leu188= | |
ENST00000263321.5:c.562C>T | ENSP00000263321.4:p.Leu188= | |
ENST00000526139.1:n.623C>T | ||
NM_000372.4:c.562C>T | NP_000363.1:p.Leu188= | |
XM_011542970.1:c.562C>T | XP_011541272.1:p.Leu188= | |
XM_011542970.2:c.562C>T | XP_011541272.1:p.Leu188= | |
XR_001748321.1:n.2718-64982G>A | ||
XR_001748322.1:n.2733-64982G>A | ||
NM_000372.5:c.562C>T MANE Select | NP_000363.1:p.Leu188= |