Canonical Allele Identifier: CA11487201
Gene: LINC02068 HGNC NCBI

Linked Data

dbSNP Id: rs2286983

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172574694G>A , CM000665.2:g.172574694G>A GRCh38
NC_000003.11:g.172292484G>A , CM000665.1:g.172292484G>A GRCh37
NC_000003.10:g.173775178G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_146714.1:n.327-354C>T