Canonical Allele Identifier: CA232144128

Gene: LINC02714

Linked Data

• dbSNP Id: rs916611411
• MyVariant Identifiers: chr11:g.134626962G>A (hg19) ; chr11:g.134757068G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757068G>A , CM000673.2:g.134757068G>A	GRCh38
NC_000011.9:g.134626962G>A , CM000673.1:g.134626962G>A	GRCh37
NC_000011.8:g.134132172G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4006G>A