Canonical Allele Identifier: CA2682575313
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189484-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189484G>T , CM000669.2:g.44189484G>T GRCh38
NC_000007.13:g.44229083G>T , CM000669.1:g.44229083G>T GRCh37
NC_000007.12:g.44195608G>T NCBI36
NG_008847.1:g.4940C>A
NG_008847.2:g.13687C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000476008.1:n.480+8207C>A
Search 100 bp 5'
Search 100 bp 3'