Canonical Allele Identifier: CA603029880
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1175492835

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756948del , CM000673.2:g.134756948del GRCh38
NC_000011.9:g.134626842del , CM000673.1:g.134626842del GRCh37
NC_000011.8:g.134132052del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4126del