Canonical Allele Identifier: CA611135016

Gene: LINC00331

Linked Data

• dbSNP Id: rs1394212021
• gnomAD v2: 13-79410600-A-C
• gnomAD v3: 13-78836465-A-C
• gnomAD v4: 13-78836465-A-C
• MyVariant Identifiers: chr13:g.79410600A>C (hg19) ; chr13:g.78836465A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836465A>C , CM000675.2:g.78836465A>C	GRCh38
NC_000013.10:g.79410600A>C , CM000675.1:g.79410600A>C	GRCh37
NC_000013.9:g.78308601A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3475T>G