Canonical Allele Identifier: CA527066325
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1309643166
gnomAD v2: 1-165448142-AG-A
gnomAD v3: 1-165478905-AG-A
gnomAD v4: 1-165478905-AG-A
MyVariant Identifiers: chr1:g.165448143del (hg19) chr1:g.165478906del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478907del , CM000663.2:g.165478907del GRCh38
NC_000001.10:g.165448144del , CM000663.1:g.165448144del GRCh37
NC_000001.9:g.163714768del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1791del
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Search 100 bp 3'