Canonical Allele Identifier: CA15147293
Gene: LINC01768 HGNC NCBI

Linked Data

dbSNP Id: rs6537883

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109862649T>C , CM000663.2:g.109862649T>C GRCh38
NC_000001.10:g.110405271T>C , CM000663.1:g.110405271T>C GRCh37
NC_000001.9:g.110206794T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738180.2:n.845+29234T>C