Canonical Allele Identifier: CA2682574929
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189374-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189374A>G , CM000669.2:g.44189374A>G GRCh38
NC_000007.13:g.44228973A>G , CM000669.1:g.44228973A>G GRCh37
NC_000007.12:g.44195498A>G NCBI36
NG_008847.1:g.5050T>C
NG_008847.2:g.13797T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-421T>C ENSP00000482149.2:n.-421T>C
ENST00000682635.1:n.66T>C
ENST00000403799.8:c.-421T>C MANE Select ENSP00000384247.3:n.-421T>C
ENST00000671824.1:c.-421T>C ENSP00000500264.1:n.-421T>C
ENST00000673284.1:c.-421T>C ENSP00000499852.1:n.-421T>C
ENST00000403799.7:c.-421T>C ENSP00000384247.3:n.-421T>C
ENST00000476008.1:n.480+8317T>C
NM_000162.3:c.-421T>C NP_000153.1:n.-421T>C
NM_000162.4:c.-421T>C NP_000153.1:n.-421T>C
NM_001354800.1:c.-421T>C NP_001341729.1:n.-421T>C
NM_000162.5:c.-421T>C MANE Select NP_000153.1:n.-421T>C
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