ClinGen Allele Registry
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Canonical Allele Identifier:
CA901232178
Gene: LINC00880
HGNC
NCBI
Linked Data
dbSNP Id:
rs1457126237
MyVariant Identifiers:
chr3:g.156836930T>C (hg19)
chr3:g.157119141T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.157119141T>C , CM000665.2:g.157119141T>C
GRCh38
NC_000003.11:g.156836930T>C , CM000665.1:g.156836930T>C
GRCh37
NC_000003.10:g.158319624T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_034007.1:n.127+3735A>G
Search 100 bp 5'
Search 100 bp 3'