Canonical Allele Identifier: CA2682575276
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189471-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189471C>A , CM000669.2:g.44189471C>A GRCh38
NC_000007.13:g.44229070C>A , CM000669.1:g.44229070C>A GRCh37
NC_000007.12:g.44195595C>A NCBI36
NG_008847.1:g.4953G>T
NG_008847.2:g.13700G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8220G>T
Search 100 bp 5'
Search 100 bp 3'