HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942193A>G , CM000672.2:g.94942193A>G | GRCh38 |
NC_000010.10:g.96701950A>G , CM000672.1:g.96701950A>G | GRCh37 |
NC_000010.9:g.96691940A>G | NCBI36 |
NG_008385.1:g.8536A>G | |
NG_008385.2:g.9036A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.333A>G MANE Select | ENSP00000260682.6:p.Gly111= | |
ENST00000643112.1:c.333A>G | ENSP00000496202.1:p.Gly111= | |
ENST00000645207.1:n.486A>G | ||
ENST00000260682.6:c.333A>G | ENSP00000260682.6:p.Gly111= | |
ENST00000461906.1:n.358A>G | ||
ENST00000473496.1:n.104A>G | ||
NM_000771.3:c.333A>G | NP_000762.2:p.Gly111= | |
NM_000771.4:c.333A>G MANE Select | NP_000762.2:p.Gly111= |