Canonical Allele Identifier: CA15665572
Gene: LINC02625 HGNC NCBI

Linked Data

dbSNP Id: rs751891

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61781965G>T , CM000672.2:g.61781965G>T GRCh38
NC_000010.10:g.63541723G>T , CM000672.1:g.63541723G>T GRCh37
NC_000010.9:g.63211729G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001747458.1:n.436-126C>A
XR_001747459.1:n.559-126C>A
XR_001747460.1:n.597-126C>A
XR_001747461.1:n.435+263C>A
XR_001747462.1:n.527-126C>A
XR_001747463.1:n.326-126C>A
XR_002957080.1:n.558+263C>A
XR_002957081.1:n.396+263C>A