Canonical Allele Identifier: CA611135017

Gene: LINC00331

Linked Data

• dbSNP Id: rs1382707825
• gnomAD v2: 13-79410648-G-A
• gnomAD v3: 13-78836513-G-A
• gnomAD v4: 13-78836513-G-A
• MyVariant Identifiers: chr13:g.79410648G>A (hg19) ; chr13:g.78836513G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836513G>A , CM000675.2:g.78836513G>A	GRCh38
NC_000013.10:g.79410648G>A , CM000675.1:g.79410648G>A	GRCh37
NC_000013.9:g.78308649G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3427C>T