ClinGen Allele Registry
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Canonical Allele Identifier:
CA901232172
Gene: LINC00880
HGNC
NCBI
Linked Data
dbSNP Id:
rs1442674448
gnomAD v3:
3-157119130-A-G
gnomAD v4:
3-157119130-A-G
MyVariant Identifiers:
chr3:g.156836919A>G (hg19)
chr3:g.157119130A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.157119130A>G , CM000665.2:g.157119130A>G
GRCh38
NC_000003.11:g.156836919A>G , CM000665.1:g.156836919A>G
GRCh37
NC_000003.10:g.158319613A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_034007.1:n.127+3746T>C
Search 100 bp 5'
Search 100 bp 3'