Canonical Allele Identifier: CA11020141
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs2886767
gnomAD v2: 2-85920329-T-C
gnomAD v3: 2-85693206-T-C
gnomAD v4: 2-85693206-T-C
MyVariant Identifiers: chr2:g.85920329T>C (hg19) chr2:g.85693206T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693206T>C , CM000664.2:g.85693206T>C GRCh38
NC_000002.11:g.85920329T>C , CM000664.1:g.85920329T>C GRCh37
NC_000002.10:g.85773840T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2114T>C
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