Canonical Allele Identifier: CA611135011

Gene: LINC00331

Linked Data

• dbSNP Id: rs1324126997
• gnomAD v2: 13-79410408-A-T
• gnomAD v3: 13-78836273-A-T
• gnomAD v4: 13-78836273-A-T
• MyVariant Identifiers: chr13:g.79410408A>T (hg19) ; chr13:g.78836273A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836273A>T , CM000675.2:g.78836273A>T	GRCh38
NC_000013.10:g.79410408A>T , CM000675.1:g.79410408A>T	GRCh37
NC_000013.9:g.78308409A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3667T>A