Canonical Allele Identifier: CA534186573

Gene: GNLY

Linked Data

• dbSNP Id: rs1255615119
• gnomAD v2: 2-85920278-A-C
• gnomAD v3: 2-85693155-A-C
• gnomAD v4: 2-85693155-A-C
• MyVariant Identifiers: chr2:g.85920278A>C (hg19) ; chr2:g.85693155A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85693155A>C , CM000664.2:g.85693155A>C	GRCh38
NC_000002.11:g.85920278A>C , CM000664.1:g.85920278A>C	GRCh37
NC_000002.10:g.85773789A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488945.5:n.48-2165A>C