Canonical Allele Identifier: CA706884489

Gene: LINC02331

Linked Data

• dbSNP Id: rs187689496
• gnomAD v3: 14-53824163-A-T
• gnomAD v4: 14-53824163-A-T
• MyVariant Identifiers: chr14:g.54290881A>T (hg19) ; chr14:g.53824163A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53824163A>T , CM000676.2:g.53824163A>T	GRCh38
NC_000014.8:g.54290881A>T , CM000676.1:g.54290881A>T	GRCh37
NC_000014.7:g.53360631A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943872.1:n.392+25559T>A
XR_943873.1:n.299+25652T>A
XR_943874.1:n.392+25559T>A
XR_943875.1:n.392+25559T>A
XR_943878.1:n.330-50341A>T
XR_001750967.2:n.416+25559T>A
XR_001750968.1:n.324+25652T>A
XR_943872.3:n.415+25559T>A
XR_943873.2:n.322+25652T>A
XR_943874.3:n.419+25559T>A