ClinGen Allele Registry
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Canonical Allele Identifier:
CA547365202
Gene: LINC00880
HGNC
NCBI
Linked Data
dbSNP Id:
rs1244270850
gnomAD v2:
3-156836908-T-A
gnomAD v3:
3-157119119-T-A
gnomAD v4:
3-157119119-T-A
MyVariant Identifiers:
chr3:g.156836908T>A (hg19)
chr3:g.157119119T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.157119119T>A , CM000665.2:g.157119119T>A
GRCh38
NC_000003.11:g.156836908T>A , CM000665.1:g.156836908T>A
GRCh37
NC_000003.10:g.158319602T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_034007.1:n.127+3757A>T
Search 100 bp 5'
Search 100 bp 3'