Canonical Allele Identifier: CA2682575285

Gene: GCK

Linked Data

• gnomAD v4: 7-44189476-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189476G>T , CM000669.2:g.44189476G>T	GRCh38
NC_000007.13:g.44229075G>T , CM000669.1:g.44229075G>T	GRCh37
NC_000007.12:g.44195600G>T	NCBI36
NG_008847.1:g.4948C>A
NG_008847.2:g.13695C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000476008.1:n.480+8215C>A