Canonical Allele Identifier: CA32228023
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs923148407
gnomAD v3: 1-165478797-T-G
gnomAD v4: 1-165478797-T-G
MyVariant Identifiers: chr1:g.165448034T>G (hg19) chr1:g.165478797T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478797T>G , CM000663.2:g.165478797T>G GRCh38
NC_000001.10:g.165448034T>G , CM000663.1:g.165448034T>G GRCh37
NC_000001.9:g.163714658T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1682A>C
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