Canonical Allele Identifier: CA534186579
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs1413112513
gnomAD v2: 2-85920347-C-G
gnomAD v3: 2-85693224-C-G
gnomAD v4: 2-85693224-C-G
MyVariant Identifiers: chr2:g.85920347C>G (hg19) chr2:g.85693224C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693224C>G , CM000664.2:g.85693224C>G GRCh38
NC_000002.11:g.85920347C>G , CM000664.1:g.85920347C>G GRCh37
NC_000002.10:g.85773858C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2096C>G
Search 100 bp 5'
Search 100 bp 3'