HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178513C>G , CM000673.2:g.89178513C>G | GRCh38 |
NC_000011.9:g.88911681C>G , CM000673.1:g.88911681C>G | GRCh37 |
NC_000011.8:g.88551329C>G | NCBI36 |
NG_008748.1:g.5642C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.560C>G MANE Select | ENSP00000263321.4:p.Ala187Gly | |
ENST00000263321.5:c.560C>G | ENSP00000263321.4:p.Ala187Gly | |
ENST00000526139.1:n.621C>G | ||
NM_000372.4:c.560C>G | NP_000363.1:p.Ala187Gly | |
XM_011542970.1:c.560C>G | XP_011541272.1:p.Ala187Gly | |
XM_011542970.2:c.560C>G | XP_011541272.1:p.Ala187Gly | |
XR_001748321.1:n.2718-64980G>C | ||
XR_001748322.1:n.2733-64980G>C | ||
NM_000372.5:c.560C>G MANE Select | NP_000363.1:p.Ala187Gly |