Canonical Allele Identifier: CA1033067326
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs1678299530
gnomAD v3: 2-85693275-A-G
gnomAD v4: 2-85693275-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693275A>G , CM000664.2:g.85693275A>G GRCh38
NC_000002.11:g.85920398A>G , CM000664.1:g.85920398A>G GRCh37
NC_000002.10:g.85773909A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2045A>G