Canonical Allele Identifier: CA2137750397
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1041749853
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53823967C>A , CM000676.2:g.53823967C>A GRCh38
NC_000014.8:g.54290685C>A , CM000676.1:g.54290685C>A GRCh37
NC_000014.7:g.53360435C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25755G>T
XR_943873.1:n.299+25848G>T
XR_943874.1:n.392+25755G>T
XR_943875.1:n.392+25755G>T
XR_943878.1:n.330-50537C>A
XR_001750967.2:n.416+25755G>T
XR_001750968.1:n.324+25848G>T
XR_943872.3:n.415+25755G>T
XR_943873.2:n.322+25848G>T
XR_943874.3:n.419+25755G>T
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