Canonical Allele Identifier: CA1055324401
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1737285041
gnomAD v3: 3-157119336-G-A
gnomAD v4: 3-157119336-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119336G>A , CM000665.2:g.157119336G>A GRCh38
NC_000003.11:g.156837125G>A , CM000665.1:g.156837125G>A GRCh37
NC_000003.10:g.158319819G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3540C>T
Search 100 bp 5'
Search 100 bp 3'