Canonical Allele Identifier: CA2725478901
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs2136512118

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134757128A>G , CM000673.2:g.134757128A>G GRCh38
NC_000011.9:g.134627022A>G , CM000673.1:g.134627022A>G GRCh37
NC_000011.8:g.134132232A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-3946A>G