Canonical Allele Identifier: CA1703654804
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44191617T= , CM000669.2:g.44191617T= GRCh38
NC_000007.13:g.44231216T= , CM000669.1:g.44231216T= GRCh37
NC_000007.12:g.44197741T= NCBI36
NG_008847.1:g.2807A=
NG_008847.2:g.11554A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476008.1:n.480+6074A=