Canonical Allele Identifier: CA253224621

Gene: LINC00331

Linked Data

• dbSNP Id: rs962159920
• MyVariant Identifiers: chr13:g.79410431A>G (hg19) ; chr13:g.78836296A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836296A>G , CM000675.2:g.78836296A>G	GRCh38
NC_000013.10:g.79410431A>G , CM000675.1:g.79410431A>G	GRCh37
NC_000013.9:g.78308432A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3644T>C