Canonical Allele Identifier: CA15201499
Gene: LINC01880 HGNC NCBI

Linked Data

dbSNP Id: rs749924

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.242084344C>T , CM000664.2:g.242084344C>T GRCh38
NC_000002.11:g.243026495C>T , CM000664.1:g.243026495C>T GRCh37
NC_000002.10:g.242675168C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924078.1:n.249G>A
XR_924079.1:n.249G>A
XR_924080.1:n.249G>A
XR_924081.1:n.249G>A
XR_924082.1:n.249G>A
XR_924083.1:n.249G>A
XR_924084.1:n.249G>A
XR_924085.1:n.249G>A