Canonical Allele Identifier: CA1055324395
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1737284997
gnomAD v3: 3-157119335-G-C
gnomAD v4: 3-157119335-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119335G>C , CM000665.2:g.157119335G>C GRCh38
NC_000003.11:g.156837124G>C , CM000665.1:g.156837124G>C GRCh37
NC_000003.10:g.158319818G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3541C>G
Search 100 bp 5'
Search 100 bp 3'