Canonical Allele Identifier: CA701182696

Gene: LINC00331

Linked Data

• dbSNP Id: rs1285527211
• MyVariant Identifiers: chr13:g.79410644G>A (hg19) ; chr13:g.78836509G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836509G>A , CM000675.2:g.78836509G>A	GRCh38
NC_000013.10:g.79410644G>A , CM000675.1:g.79410644G>A	GRCh37
NC_000013.9:g.78308645G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3431C>T