Canonical Allele Identifier: CA2011125388
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939612572

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756968A>G , CM000673.2:g.134756968A>G GRCh38
NC_000011.9:g.134626862A>G , CM000673.1:g.134626862A>G GRCh37
NC_000011.8:g.134132072A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4106A>G