Canonical Allele Identifier: CA701182688

Gene: LINC00331

Linked Data

• dbSNP Id: rs1177503316
• gnomAD v3: 13-78836494-C-T
• gnomAD v4: 13-78836494-C-T
• MyVariant Identifiers: chr13:g.79410629C>T (hg19) ; chr13:g.78836494C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836494C>T , CM000675.2:g.78836494C>T	GRCh38
NC_000013.10:g.79410629C>T , CM000675.1:g.79410629C>T	GRCh37
NC_000013.9:g.78308630C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3446G>A