Canonical Allele Identifier: CA253224652

Gene: LINC00331

Linked Data

• dbSNP Id: rs898022416
• gnomAD v2: 13-79410727-TG-T
• gnomAD v3: 13-78836592-TG-T
• gnomAD v4: 13-78836592-TG-T
• MyVariant Identifiers: chr13:g.79410728del (hg19) ; chr13:g.78836593del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836593del , CM000675.2:g.78836593del	GRCh38
NC_000013.10:g.79410728del , CM000675.1:g.79410728del	GRCh37
NC_000013.9:g.78308729del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3347del