Canonical Allele Identifier: CA253224661

Gene: LINC00331

Linked Data

• dbSNP Id: rs78740613
• gnomAD v2: 13-79410789-C-T
• gnomAD v3: 13-78836654-C-T
• gnomAD v4: 13-78836654-C-T
• MyVariant Identifiers: chr13:g.79410789C>T (hg19) ; chr13:g.78836654C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836654C>T , CM000675.2:g.78836654C>T	GRCh38
NC_000013.10:g.79410789C>T , CM000675.1:g.79410789C>T	GRCh37
NC_000013.9:g.78308790C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3286G>A