Canonical Allele Identifier: CA706884468
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1265818603
gnomAD v3: 14-53824144-A-G
gnomAD v4: 14-53824144-A-G
MyVariant Identifiers: chr14:g.54290862A>G (hg19) chr14:g.53824144A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824144A>G , CM000676.2:g.53824144A>G GRCh38
NC_000014.8:g.54290862A>G , CM000676.1:g.54290862A>G GRCh37
NC_000014.7:g.53360612A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25578T>C
XR_943873.1:n.299+25671T>C
XR_943874.1:n.392+25578T>C
XR_943875.1:n.392+25578T>C
XR_943878.1:n.330-50360A>G
XR_001750967.2:n.416+25578T>C
XR_001750968.1:n.324+25671T>C
XR_943872.3:n.415+25578T>C
XR_943873.2:n.322+25671T>C
XR_943874.3:n.419+25578T>C
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