Canonical Allele Identifier: CA32228005
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs945063636
MyVariant Identifiers: chr1:g.165478663A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478663A>T , CM000663.2:g.165478663A>T GRCh38
NC_000001.10:g.165447900A>T , CM000663.1:g.165447900A>T GRCh37
NC_000001.9:g.163714524A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026744.2:n.1530-1548T>A