Canonical Allele Identifier: CA86469735
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs576991279
gnomAD v3: 3-157119059-G-C
gnomAD v4: 3-157119059-G-C
MyVariant Identifiers: chr3:g.156836848G>C (hg19) chr3:g.157119059G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119059G>C , CM000665.2:g.157119059G>C GRCh38
NC_000003.11:g.156836848G>C , CM000665.1:g.156836848G>C GRCh37
NC_000003.10:g.158319542G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3817C>G
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