Canonical Allele Identifier: CA261458691

Gene: LINC02331

Linked Data

• dbSNP Id: rs991411546
• gnomAD v2: 14-54290845-G-C
• gnomAD v3: 14-53824127-G-C
• gnomAD v4: 14-53824127-G-C
• MyVariant Identifiers: chr14:g.54290845G>C (hg19) ; chr14:g.53824127G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53824127G>C , CM000676.2:g.53824127G>C	GRCh38
NC_000014.8:g.54290845G>C , CM000676.1:g.54290845G>C	GRCh37
NC_000014.7:g.53360595G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943872.1:n.392+25595C>G
XR_943873.1:n.299+25688C>G
XR_943874.1:n.392+25595C>G
XR_943875.1:n.392+25595C>G
XR_943878.1:n.330-50377G>C
XR_001750967.2:n.416+25595C>G
XR_001750968.1:n.324+25688C>G
XR_943872.3:n.415+25595C>G
XR_943873.2:n.322+25688C>G
XR_943874.3:n.419+25595C>G