Canonical Allele Identifier: CA197961763

Gene: LINC01492

Linked Data

• dbSNP Id: rs750248415
• MyVariant Identifiers: chr9:g.106024057A>G (hg19) ; chr9:g.103261775A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261775A>G , CM000671.2:g.103261775A>G	GRCh38
NC_000009.11:g.106024057A>G , CM000671.1:g.106024057A>G	GRCh37
NC_000009.10:g.105063878A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2749T>C