Canonical Allele Identifier: CA14624368
Gene: LINC01905 HGNC NCBI
LINC03069 HGNC NCBI

Linked Data

dbSNP Id: rs2286812

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.56050233C>T , CM000680.2:g.56050233C>T GRCh38
NC_000018.9:g.53717464C>T , CM000680.1:g.53717464C>T GRCh37
NC_000018.8:g.51868462C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_146510.1:n.165+56C>T (LINC01905)
NR_146511.1:n.165+56C>T (LINC01905)
NR_148972.1:n.1067+5672G>A (LINC03069)