Canonical Allele Identifier: CA527066318
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1243827206
gnomAD v2: 1-165447955-C-CT
gnomAD v3: 1-165478718-C-CT
gnomAD v4: 1-165478718-C-CT
MyVariant Identifiers: chr1:g.165447956_165447957insT (hg19) chr1:g.165447955_165447956insT (hg19) chr1:g.165478719_165478720insT (hg38) chr1:g.165478718_165478719insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478727dup , CM000663.2:g.165478727dup GRCh38
NC_000001.10:g.165447964dup , CM000663.1:g.165447964dup GRCh37
NC_000001.9:g.163714588dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026744.2:n.1530-1604dup
Search 100 bp 5'
Search 100 bp 3'