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Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.46725231T>G , CM000682.2:g.46725231T>G
GRCh38
NC_000020.10:g.45353870T>G , CM000682.1:g.45353870T>G
GRCh37
NC_000020.9:g.44787277T>G
NCBI36
NG_016284.1:g.20592T>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000359271.4:c.195T>G
MANE Select
ENSP00000352216.2:p.Gly65=
ENST00000359271.3:c.195T>G
ENSP00000352216.2:p.Gly65=
ENST00000611837.1:n.347T>G
NM_030777.3:c.195T>G
NP_110404.1:p.Gly65=
XM_011529060.1:c.258T>G
XP_011527362.1:p.Gly86=
XM_011529061.1:c.204T>G
XP_011527363.1:p.Gly68=
XM_011529062.1:c.258T>G
XP_011527364.1:p.Gly86=
XM_011529063.1:c.258T>G
XP_011527365.1:p.Gly86=
XM_011529064.1:c.258T>G
XP_011527366.1:p.Gly86=
XM_011529065.1:c.258T>G
XP_011527367.1:p.Gly86=
XR_936641.1:n.394T>G
XM_011529060.2:c.258T>G
XP_011527362.1:p.Gly86=
XM_011529061.2:c.204T>G
XP_011527363.1:p.Gly68=
XM_011529062.2:c.258T>G
XP_011527364.1:p.Gly86=
XM_011529063.2:c.258T>G
XP_011527365.1:p.Gly86=
XM_011529064.2:c.258T>G
XP_011527366.1:p.Gly86=
XM_011529065.2:c.258T>G
XP_011527367.1:p.Gly86=
XM_017028087.2:c.195T>G
XP_016883576.1:p.Gly65=
XR_936641.2:n.381T>G
NM_030777.4:c.195T>G
MANE Select
NP_110404.1:p.Gly65=