Canonical Allele Identifier: CA51770232
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs769124770
gnomAD v2: 2-85920390-G-A
gnomAD v3: 2-85693267-G-A
gnomAD v4: 2-85693267-G-A
MyVariant Identifiers: chr2:g.85920390G>A (hg19) chr2:g.85693267G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693267G>A , CM000664.2:g.85693267G>A GRCh38
NC_000002.11:g.85920390G>A , CM000664.1:g.85920390G>A GRCh37
NC_000002.10:g.85773901G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2053G>A
Search 100 bp 5'
Search 100 bp 3'