Canonical Allele Identifier: CA857924188

Gene: LINC01492

Linked Data

• dbSNP Id: rs1290021084
• MyVariant Identifiers: chr9:g.106024206del (hg19) ; chr9:g.103261924del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261924del , CM000671.2:g.103261924del	GRCh38
NC_000009.11:g.106024206del , CM000671.1:g.106024206del	GRCh37
NC_000009.10:g.105064027del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2600del