Canonical Allele Identifier: CA157886330

Gene: GCK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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