Canonical Allele Identifier: CA706884528

Gene: LINC02331

Linked Data

• dbSNP Id: rs1463210078
• MyVariant Identifiers: chr14:g.54290951A>C (hg19) ; chr14:g.53824233A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53824233A>C , CM000676.2:g.53824233A>C	GRCh38
NC_000014.8:g.54290951A>C , CM000676.1:g.54290951A>C	GRCh37
NC_000014.7:g.53360701A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943872.1:n.392+25489T>G
XR_943873.1:n.299+25582T>G
XR_943874.1:n.392+25489T>G
XR_943875.1:n.392+25489T>G
XR_943878.1:n.330-50271A>C
XR_001750967.2:n.416+25489T>G
XR_001750968.1:n.324+25582T>G
XR_943872.3:n.415+25489T>G
XR_943873.2:n.322+25582T>G
XR_943874.3:n.419+25489T>G