HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178903A= , CM000673.2:g.89178903A= | GRCh38 |
NC_000011.9:g.88912071A= , CM000673.1:g.88912071A= | GRCh37 |
NC_000011.8:g.88551719A= | NCBI36 |
NG_008748.1:g.6032A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.819+131A= MANE Select | ENSP00000263321.4:n.819+131A= | |
ENST00000263321.5:c.819+131A= | ENSP00000263321.4:n.819+131A= | |
ENST00000526139.1:n.880+131A= | ||
NM_000372.4:c.819+131A= | NP_000363.1:n.819+131A= | |
XM_011542970.1:c.819+131A= | XP_011541272.1:n.819+131A= | |
XM_011542970.2:c.819+131A= | XP_011541272.1:n.819+131A= | |
XR_001748321.1:n.2718-65370T= | ||
XR_001748322.1:n.2733-65370T= | ||
NM_000372.5:c.819+131A= MANE Select | NP_000363.1:n.819+131A= |