Canonical Allele Identifier: CA2704270629
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs2108089762

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119257T>G , CM000665.2:g.157119257T>G GRCh38
NC_000003.11:g.156837046T>G , CM000665.1:g.156837046T>G GRCh37
NC_000003.10:g.158319740T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3619A>C