ClinGen Allele Registry
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Canonical Allele Identifier:
CA1033067238
Gene: GNLY
HGNC
NCBI
Linked Data
dbSNP Id:
rs1678292998
gnomAD v3:
2-85693146-C-CA
gnomAD v4:
2-85693146-C-CA
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.85693147dup , CM000664.2:g.85693147dup
GRCh38
NC_000002.11:g.85920270dup , CM000664.1:g.85920270dup
GRCh37
NC_000002.10:g.85773781dup
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000488945.5:n.48-2173dup
Search 100 bp 5'
Search 100 bp 3'