Canonical Allele Identifier: CA1055324251
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1737282521
gnomAD v3: 3-157119129-C-T
gnomAD v4: 3-157119129-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119129C>T , CM000665.2:g.157119129C>T GRCh38
NC_000003.11:g.156836918C>T , CM000665.1:g.156836918C>T GRCh37
NC_000003.10:g.158319612C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3747G>A
Search 100 bp 5'
Search 100 bp 3'