Canonical Allele Identifier: CA2714284186
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2096324916
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189375T>C , CM000669.2:g.44189375T>C GRCh38
NC_000007.13:g.44228974T>C , CM000669.1:g.44228974T>C GRCh37
NC_000007.12:g.44195499T>C NCBI36
NG_008847.1:g.5049A>G
NG_008847.2:g.13796A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-422A>G ENSP00000482149.2:n.-422A>G
ENST00000682635.1:n.65A>G
ENST00000403799.8:c.-422A>G MANE Select ENSP00000384247.3:n.-422A>G
ENST00000671824.1:c.-422A>G ENSP00000500264.1:n.-422A>G
ENST00000673284.1:c.-422A>G ENSP00000499852.1:n.-422A>G
ENST00000403799.7:c.-422A>G ENSP00000384247.3:n.-422A>G
ENST00000476008.1:n.480+8316A>G
NM_000162.3:c.-422A>G NP_000153.1:n.-422A>G
NM_000162.4:c.-422A>G NP_000153.1:n.-422A>G
NM_001354800.1:c.-422A>G NP_001341729.1:n.-422A>G
NM_000162.5:c.-422A>G MANE Select NP_000153.1:n.-422A>G
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