Canonical Allele Identifier: CA890580008
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1222729668
gnomAD v3: 1-165478992-G-C
gnomAD v4: 1-165478992-G-C
MyVariant Identifiers: chr1:g.165448229G>C (hg19) chr1:g.165478992G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478992G>C , CM000663.2:g.165478992G>C GRCh38
NC_000001.10:g.165448229G>C , CM000663.1:g.165448229G>C GRCh37
NC_000001.9:g.163714853G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1877C>G
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