Canonical Allele Identifier: CA86469729
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs927322453
gnomAD v2: 3-156836806-T-C
gnomAD v3: 3-157119017-T-C
gnomAD v4: 3-157119017-T-C
MyVariant Identifiers: chr3:g.156836806T>C (hg19) chr3:g.157119017T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119017T>C , CM000665.2:g.157119017T>C GRCh38
NC_000003.11:g.156836806T>C , CM000665.1:g.156836806T>C GRCh37
NC_000003.10:g.158319500T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3859A>G
Search 100 bp 5'
Search 100 bp 3'