Canonical Allele Identifier: CA2682575316

Gene: GCK

Linked Data

• gnomAD v4: 7-44189486-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189486G>T , CM000669.2:g.44189486G>T	GRCh38
NC_000007.13:g.44229085G>T , CM000669.1:g.44229085G>T	GRCh37
NC_000007.12:g.44195610G>T	NCBI36
NG_008847.1:g.4938C>A
NG_008847.2:g.13685C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000476008.1:n.480+8205C>A