Canonical Allele Identifier: CA261458677

Gene: LINC02331

Linked Data

• dbSNP Id: rs1029079277
• MyVariant Identifiers: chr14:g.54290716C>G (hg19) ; chr14:g.53823998C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53823998C>G , CM000676.2:g.53823998C>G	GRCh38
NC_000014.8:g.54290716C>G , CM000676.1:g.54290716C>G	GRCh37
NC_000014.7:g.53360466C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943872.1:n.392+25724G>C
XR_943873.1:n.299+25817G>C
XR_943874.1:n.392+25724G>C
XR_943875.1:n.392+25724G>C
XR_943878.1:n.330-50506C>G
XR_001750967.2:n.416+25724G>C
XR_001750968.1:n.324+25817G>C
XR_943872.3:n.415+25724G>C
XR_943873.2:n.322+25817G>C
XR_943874.3:n.419+25724G>C