Canonical Allele Identifier: CA1703653874
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189480G= , CM000669.2:g.44189480G= GRCh38
NC_000007.13:g.44229079G= , CM000669.1:g.44229079G= GRCh37
NC_000007.12:g.44195604G= NCBI36
NG_008847.1:g.4944C=
NG_008847.2:g.13691C=

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8211C=