Canonical Allele Identifier: CA706884563
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1261567630
MyVariant Identifiers: chr14:g.54290991G>A (hg19) chr14:g.53824273G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824273G>A , CM000676.2:g.53824273G>A GRCh38
NC_000014.8:g.54290991G>A , CM000676.1:g.54290991G>A GRCh37
NC_000014.7:g.53360741G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25449C>T
XR_943873.1:n.299+25542C>T
XR_943874.1:n.392+25449C>T
XR_943875.1:n.392+25449C>T
XR_943878.1:n.330-50231G>A
XR_001750967.2:n.416+25449C>T
XR_001750968.1:n.324+25542C>T
XR_943872.3:n.415+25449C>T
XR_943873.2:n.322+25542C>T
XR_943874.3:n.419+25449C>T
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