ClinGen Allele Registry
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Canonical Allele Identifier:
CA321892229
Gene: LINC00163
HGNC
NCBI
Linked Data
dbSNP Id:
rs13046884
gnomAD v2:
21-46413645-A-G
gnomAD v3:
21-44993730-A-G
gnomAD v4:
21-44993730-A-G
MyVariant Identifiers:
chr21:g.46413645A>G (hg19)
chr21:g.44993730A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.44993730A>G , CM000683.2:g.44993730A>G
GRCh38
NC_000021.8:g.46413645A>G , CM000683.1:g.46413645A>G
GRCh37
NC_000021.7:g.45238073A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_033840.1:n.183+174T>C
Search 100 bp 5'
Search 100 bp 3'