Canonical Allele Identifier: CA943861433
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939611777

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756888G>C , CM000673.2:g.134756888G>C GRCh38
NC_000011.9:g.134626782G>C , CM000673.1:g.134626782G>C GRCh37
NC_000011.8:g.134131992G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4186G>C