Canonical Allele Identifier: CA589962189

Gene: LINC01492

Linked Data

• dbSNP Id: rs1210953575
• gnomAD v2: 9-106024074-G-A
• gnomAD v3: 9-103261792-G-A
• gnomAD v4: 9-103261792-G-A
• MyVariant Identifiers: chr9:g.106024074G>A (hg19) ; chr9:g.103261792G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261792G>A , CM000671.2:g.103261792G>A	GRCh38
NC_000009.11:g.106024074G>A , CM000671.1:g.106024074G>A	GRCh37
NC_000009.10:g.105063895G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2732C>T