Canonical Allele Identifier: CA2714459758

Gene: GCK

Linked Data

• dbSNP Id: rs2128835024

Genomic Alleles

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

Transcript Alleles

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