Canonical Allele Identifier: CA857924173

Gene: LINC01492

Linked Data

• dbSNP Id: rs1283742561
• gnomAD v3: 9-103261819-T-A
• gnomAD v4: 9-103261819-T-A
• MyVariant Identifiers: chr9:g.106024101T>A (hg19) ; chr9:g.103261819T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261819T>A , CM000671.2:g.103261819T>A	GRCh38
NC_000009.11:g.106024101T>A , CM000671.1:g.106024101T>A	GRCh37
NC_000009.10:g.105063922T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2705A>T