Canonical Allele Identifier: CA253224649

Gene: LINC00331

Linked Data

• dbSNP Id: rs562078235
• gnomAD v2: 13-79410692-A-G
• gnomAD v3: 13-78836557-A-G
• gnomAD v4: 13-78836557-A-G
• MyVariant Identifiers: chr13:g.79410692A>G (hg19) ; chr13:g.78836557A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836557A>G , CM000675.2:g.78836557A>G	GRCh38
NC_000013.10:g.79410692A>G , CM000675.1:g.79410692A>G	GRCh37
NC_000013.9:g.78308693A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3383T>C