Canonical Allele Identifier: CA534186585
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs1277701430
gnomAD v2: 2-85920427-C-T
gnomAD v3: 2-85693304-C-T
gnomAD v4: 2-85693304-C-T
MyVariant Identifiers: chr2:g.85920427C>T (hg19) chr2:g.85693304C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693304C>T , CM000664.2:g.85693304C>T GRCh38
NC_000002.11:g.85920427C>T , CM000664.1:g.85920427C>T GRCh37
NC_000002.10:g.85773938C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2016C>T
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