Canonical Allele Identifier: CA213771
Gene: GCK HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 36209
dbSNP Id: rs193922289

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44152420C>T , CM000669.2:g.44152420C>T GRCh38
NC_000007.13:g.44192019C>T , CM000669.1:g.44192019C>T GRCh37
NC_000007.12:g.44158544C>T NCBI36
NG_008847.1:g.42004G>A
NG_008847.2:g.50751G>A

Transcript Alleles

HGVS Amino-acid change
NM_000162.3:c.214G>A VV NP_000153.1:p.Gly72Arg
NM_033507.1:c.217G>A VV NP_277042.1:p.Gly73Arg
NM_033508.1:c.211G>A VV NP_277043.1:p.Gly71Arg
NM_000162.4:c.214G>A VV
NM_001354800.1:c.214G>A VV NP_001341729.1:p.Gly72Arg
NM_033507.2:c.217G>A VV
NM_033508.2:c.211G>A VV
NM_000162.5:c.214G>A VV MANE Preferred
ENST00000345378.6:c.217G>A ENSP00000223366.2:p.Gly73Arg
ENST00000395796.7:c.211G>A ENSP00000379142.3:p.Gly71Arg
ENST00000403799.7:c.214G>A ENSP00000384247.3:p.Gly72Arg
ENST00000437084.1:c.214G>A ENSP00000402840.1:p.Gly72Arg
ENST00000616242.4:n.211G>A ENSP00000482149.1:p.Gly71Arg