Canonical Allele Identifier: CA2682575311
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189483-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189483T>C , CM000669.2:g.44189483T>C GRCh38
NC_000007.13:g.44229082T>C , CM000669.1:g.44229082T>C GRCh37
NC_000007.12:g.44195607T>C NCBI36
NG_008847.1:g.4941A>G
NG_008847.2:g.13688A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8208A>G