Canonical Allele Identifier: CA894008683

Gene: GNLY

Linked Data

• dbSNP Id: rs937855156
• gnomAD v3: 2-85693218-C-A
• gnomAD v4: 2-85693218-C-A
• MyVariant Identifiers: chr2:g.85920341C>A (hg19) ; chr2:g.85693218C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85693218C>A , CM000664.2:g.85693218C>A	GRCh38
NC_000002.11:g.85920341C>A , CM000664.1:g.85920341C>A	GRCh37
NC_000002.10:g.85773852C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488945.5:n.48-2102C>A