Canonical Allele Identifier: CA901232133
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1420532913
gnomAD v3: 3-157119053-T-C
gnomAD v4: 3-157119053-T-C
MyVariant Identifiers: chr3:g.156836842T>C (hg19) chr3:g.157119053T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119053T>C , CM000665.2:g.157119053T>C GRCh38
NC_000003.11:g.156836842T>C , CM000665.1:g.156836842T>C GRCh37
NC_000003.10:g.158319536T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3823A>G
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