ClinGen Allele Registry
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Canonical Allele Identifier:
CA890579991
Gene: LRRC52-AS1
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.165478920T>A
GRCh37
chr1:g.165448157T>A
Linked Data - NCBI & NCI
dbSNP:
10918196
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165478920T>A , CM000663.2:g.165478920T>A
GRCh38
NC_000001.10:g.165448157T>A , CM000663.1:g.165448157T>A
GRCh37
NC_000001.9:g.163714781T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026744.2:n.1530-1805A>T
Search 100 bp 5'
Search 100 bp 3'