Canonical Allele Identifier: CA957924113

Gene: LINC00331

Linked Data

• dbSNP Id: rs1880406494
• gnomAD v3: 13-78836391-C-T
• gnomAD v4: 13-78836391-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836391C>T , CM000675.2:g.78836391C>T	GRCh38
NC_000013.10:g.79410526C>T , CM000675.1:g.79410526C>T	GRCh37
NC_000013.9:g.78308527C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3549G>A