Canonical Allele Identifier: CA32228040
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs80042865
gnomAD v2: 1-165448211-T-A
gnomAD v3: 1-165478974-T-A
gnomAD v4: 1-165478974-T-A
MyVariant Identifiers: chr1:g.165448211T>A (hg19) chr1:g.165478974T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478974T>A , CM000663.2:g.165478974T>A GRCh38
NC_000001.10:g.165448211T>A , CM000663.1:g.165448211T>A GRCh37
NC_000001.9:g.163714835T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026744.2:n.1530-1859A>T
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