Canonical Allele Identifier: CA2682575291
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189477-A-T
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8214T>A
Search 100 bp 5'
Search 100 bp 3'