Canonical Allele Identifier: CA2682575312
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189483-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189483T>A , CM000669.2:g.44189483T>A GRCh38
NC_000007.13:g.44229082T>A , CM000669.1:g.44229082T>A GRCh37
NC_000007.12:g.44195607T>A NCBI36
NG_008847.1:g.4941A>T
NG_008847.2:g.13688A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8208A>T