Canonical Allele Identifier: CA890580029
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1302930612
gnomAD v3: 1-165479039-T-C
gnomAD v4: 1-165479039-T-C
MyVariant Identifiers: chr1:g.165448276T>C (hg19) chr1:g.165479039T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165479039T>C , CM000663.2:g.165479039T>C GRCh38
NC_000001.10:g.165448276T>C , CM000663.1:g.165448276T>C GRCh37
NC_000001.9:g.163714900T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026744.2:n.1530-1924A>G
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