Canonical Allele Identifier: CA2714459747
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2128835018

Genomic Alleles

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

Transcript Alleles

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