Canonical Allele Identifier: CA901232167
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1330040598
gnomAD v3: 3-157119114-G-A
gnomAD v4: 3-157119114-G-A
MyVariant Identifiers: chr3:g.156836903G>A (hg19) chr3:g.157119114G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119114G>A , CM000665.2:g.157119114G>A GRCh38
NC_000003.11:g.156836903G>A , CM000665.1:g.156836903G>A GRCh37
NC_000003.10:g.158319597G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3762C>T
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Search 100 bp 3'