Canonical Allele Identifier: CA32228018
Gene: LRRC52-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1024859643
MyVariant Identifiers: chr1:g.165448010T>C (hg19) chr1:g.165478773T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478773T>C , CM000663.2:g.165478773T>C GRCh38
NC_000001.10:g.165448010T>C , CM000663.1:g.165448010T>C GRCh37
NC_000001.9:g.163714634T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026744.2:n.1530-1658A>G
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