Canonical Allele Identifier: CA1033067123

Gene: GNLY

Linked Data

• dbSNP Id: rs980110466
• gnomAD v3: 2-85693139-C-A
• gnomAD v4: 2-85693139-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85693139C>A , CM000664.2:g.85693139C>A	GRCh38
NC_000002.11:g.85920262C>A , CM000664.1:g.85920262C>A	GRCh37
NC_000002.10:g.85773773C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488945.5:n.48-2181C>A