Canonical Allele Identifier: CA2137750344
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1893187931
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53823814T>G , CM000676.2:g.53823814T>G GRCh38
NC_000014.8:g.54290532T>G , CM000676.1:g.54290532T>G GRCh37
NC_000014.7:g.53360282T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25908A>C
XR_943873.1:n.299+26001A>C
XR_943874.1:n.392+25908A>C
XR_943875.1:n.392+25908A>C
XR_943878.1:n.330-50690T>G
XR_001750967.2:n.416+25908A>C
XR_001750968.1:n.324+26001A>C
XR_943872.3:n.415+25908A>C
XR_943873.2:n.322+26001A>C
XR_943874.3:n.419+25908A>C
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