Canonical Allele Identifier: CA1033067308
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs1573490782
gnomAD v3: 2-85693173-T-G
gnomAD v4: 2-85693173-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693173T>G , CM000664.2:g.85693173T>G GRCh38
NC_000002.11:g.85920296T>G , CM000664.1:g.85920296T>G GRCh37
NC_000002.10:g.85773807T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2147T>G