Canonical Allele Identifier: CA51770215
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs905077481
gnomAD v3: 2-85693210-C-T
gnomAD v4: 2-85693210-C-T
MyVariant Identifiers: chr2:g.85920333C>T (hg19) chr2:g.85693210C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693210C>T , CM000664.2:g.85693210C>T GRCh38
NC_000002.11:g.85920333C>T , CM000664.1:g.85920333C>T GRCh37
NC_000002.10:g.85773844C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2110C>T
Search 100 bp 5'
Search 100 bp 3'