Canonical Allele Identifier: CA894008733

Gene: GNLY

Linked Data

• dbSNP Id: rs1410698776
• MyVariant Identifiers: chr2:g.85920407A>T (hg19) ; chr2:g.85693284A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85693284A>T , CM000664.2:g.85693284A>T	GRCh38
NC_000002.11:g.85920407A>T , CM000664.1:g.85920407A>T	GRCh37
NC_000002.10:g.85773918A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488945.5:n.48-2036A>T