Canonical Allele Identifier: CA701182656

Gene: LINC00331

Linked Data

• dbSNP Id: rs1458177677
• MyVariant Identifiers: chr13:g.79410518T>C (hg19) ; chr13:g.78836383T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836383T>C , CM000675.2:g.78836383T>C	GRCh38
NC_000013.10:g.79410518T>C , CM000675.1:g.79410518T>C	GRCh37
NC_000013.9:g.78308519T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3557A>G