Canonical Allele Identifier: CA261458656
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs76316670
gnomAD v2: 14-54290530-C-T
gnomAD v3: 14-53823812-C-T
gnomAD v4: 14-53823812-C-T
MyVariant Identifiers: chr14:g.54290530C>T (hg19) chr14:g.53823812C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53823812C>T , CM000676.2:g.53823812C>T GRCh38
NC_000014.8:g.54290530C>T , CM000676.1:g.54290530C>T GRCh37
NC_000014.7:g.53360280C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25910G>A
XR_943873.1:n.299+26003G>A
XR_943874.1:n.392+25910G>A
XR_943875.1:n.392+25910G>A
XR_943878.1:n.330-50692C>T
XR_001750967.2:n.416+25910G>A
XR_001750968.1:n.324+26003G>A
XR_943872.3:n.415+25910G>A
XR_943873.2:n.322+26003G>A
XR_943874.3:n.419+25910G>A
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