Canonical Allele Identifier: CA2682575287
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189477-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189477A>C , CM000669.2:g.44189477A>C GRCh38
NC_000007.13:g.44229076A>C , CM000669.1:g.44229076A>C GRCh37
NC_000007.12:g.44195601A>C NCBI36
NG_008847.1:g.4947T>G
NG_008847.2:g.13694T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8214T>G