Canonical Allele Identifier: CA197961748

Gene: LINC01492

Linked Data

• dbSNP Id: rs377545224
• gnomAD v2: 9-106023958-C-A
• gnomAD v3: 9-103261676-C-A
• gnomAD v4: 9-103261676-C-A
• MyVariant Identifiers: chr9:g.106023958C>A (hg19) ; chr9:g.103261676C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261676C>A , CM000671.2:g.103261676C>A	GRCh38
NC_000009.11:g.106023958C>A , CM000671.1:g.106023958C>A	GRCh37
NC_000009.10:g.105063779C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2848G>T