Canonical Allele Identifier: CA701182635

Gene: LINC00331

Linked Data

• dbSNP Id: rs1171209448
• MyVariant Identifiers: chr13:g.79410480C>G (hg19) ; chr13:g.78836345C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836345C>G , CM000675.2:g.78836345C>G	GRCh38
NC_000013.10:g.79410480C>G , CM000675.1:g.79410480C>G	GRCh37
NC_000013.9:g.78308481C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3595G>C