Canonical Allele Identifier: CA706884481

Gene: LINC02331

Linked Data

• dbSNP Id: rs1197636675
• MyVariant Identifiers: chr14:g.54290866G>C (hg19) ; chr14:g.53824148G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53824148G>C , CM000676.2:g.53824148G>C	GRCh38
NC_000014.8:g.54290866G>C , CM000676.1:g.54290866G>C	GRCh37
NC_000014.7:g.53360616G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943872.1:n.392+25574C>G
XR_943873.1:n.299+25667C>G
XR_943874.1:n.392+25574C>G
XR_943875.1:n.392+25574C>G
XR_943878.1:n.330-50356G>C
XR_001750967.2:n.416+25574C>G
XR_001750968.1:n.324+25667C>G
XR_943872.3:n.415+25574C>G
XR_943873.2:n.322+25667C>G
XR_943874.3:n.419+25574C>G