Canonical Allele Identifier: CA2714459512
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2128835016

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189474G>A , CM000669.2:g.44189474G>A GRCh38
NC_000007.13:g.44229073G>A , CM000669.1:g.44229073G>A GRCh37
NC_000007.12:g.44195598G>A NCBI36
NG_008847.1:g.4950C>T
NG_008847.2:g.13697C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8217C>T