Canonical Allele Identifier: CA2682575277

Gene: GCK

Linked Data

• dbSNP Id: rs2128835014
• gnomAD v4: 7-44189471-C-T

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000476008.1:n.480+8220G>A