Canonical Allele Identifier: CA2682575306

Gene: GCK

Linked Data

• gnomAD v4: 7-44189481-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189481C>T , CM000669.2:g.44189481C>T	GRCh38
NC_000007.13:g.44229080C>T , CM000669.1:g.44229080C>T	GRCh37
NC_000007.12:g.44195605C>T	NCBI36
NG_008847.1:g.4943G>A
NG_008847.2:g.13690G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000476008.1:n.480+8210G>A