Canonical Allele Identifier: CA32228013
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs924574458
gnomAD v2: 1-165447983-C-T
gnomAD v3: 1-165478746-C-T
gnomAD v4: 1-165478746-C-T
MyVariant Identifiers: chr1:g.165447983C>T (hg19) chr1:g.165478746C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478746C>T , CM000663.2:g.165478746C>T GRCh38
NC_000001.10:g.165447983C>T , CM000663.1:g.165447983C>T GRCh37
NC_000001.9:g.163714607C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1631G>A
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