Canonical Allele Identifier: CA701182627

Gene: LINC00331

Linked Data

• dbSNP Id: rs1398190581
• MyVariant Identifiers: chr13:g.79410471_79410494del (hg19) ; chr13:g.78836336_78836359del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836347_78836370del , CM000675.2:g.78836347_78836370del	GRCh38
NC_000013.10:g.79410482_79410505del , CM000675.1:g.79410482_79410505del	GRCh37
NC_000013.9:g.78308483_78308506del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3581_111+3604del