HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178565A>T , CM000673.2:g.89178565A>T | GRCh38 |
NC_000011.9:g.88911733A>T , CM000673.1:g.88911733A>T | GRCh37 |
NC_000011.8:g.88551381A>T | NCBI36 |
NG_008748.1:g.5694A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.612A>T MANE Select | ENSP00000263321.4:p.Ala204= | |
ENST00000263321.5:c.612A>T | ENSP00000263321.4:p.Ala204= | |
ENST00000526139.1:n.673A>T | ||
NM_000372.4:c.612A>T | NP_000363.1:p.Ala204= | |
XM_011542970.1:c.612A>T | XP_011541272.1:p.Ala204= | |
XM_011542970.2:c.612A>T | XP_011541272.1:p.Ala204= | |
XR_001748321.1:n.2718-65032T>A | ||
XR_001748322.1:n.2733-65032T>A | ||
NM_000372.5:c.612A>T MANE Select | NP_000363.1:p.Ala204= |