Canonical Allele Identifier: CA1703653875
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189487G= , CM000669.2:g.44189487G= GRCh38
NC_000007.13:g.44229086G= , CM000669.1:g.44229086G= GRCh37
NC_000007.12:g.44195611G= NCBI36
NG_008847.1:g.4937C=
NG_008847.2:g.13684C=

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8204C=