Canonical Allele Identifier: CA2682575329
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189489-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189489T>G , CM000669.2:g.44189489T>G GRCh38
NC_000007.13:g.44229088T>G , CM000669.1:g.44229088T>G GRCh37
NC_000007.12:g.44195613T>G NCBI36
NG_008847.1:g.4935A>C
NG_008847.2:g.13682A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8202A>C
Search 100 bp 5'
Search 100 bp 3'