Canonical Allele Identifier: CA957924069

Gene: LINC00331

Linked Data

• dbSNP Id: rs1593865513
• gnomAD v3: 13-78836328-T-C
• gnomAD v4: 13-78836328-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836328T>C , CM000675.2:g.78836328T>C	GRCh38
NC_000013.10:g.79410463T>C , CM000675.1:g.79410463T>C	GRCh37
NC_000013.9:g.78308464T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3612A>G