Canonical Allele Identifier: CA2714459509
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2128835013

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189470T>C , CM000669.2:g.44189470T>C GRCh38
NC_000007.13:g.44229069T>C , CM000669.1:g.44229069T>C GRCh37
NC_000007.12:g.44195594T>C NCBI36
NG_008847.1:g.4954A>G
NG_008847.2:g.13701A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8221A>G