Canonical Allele Identifier: CA197961802

Gene: LINC01492

Linked Data

• dbSNP Id: rs187210995
• gnomAD v2: 9-106024211-A-T
• gnomAD v3: 9-103261929-A-T
• gnomAD v4: 9-103261929-A-T
• MyVariant Identifiers: chr9:g.106024211A>T (hg19) ; chr9:g.103261929A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261929A>T , CM000671.2:g.103261929A>T	GRCh38
NC_000009.11:g.106024211A>T , CM000671.1:g.106024211A>T	GRCh37
NC_000009.10:g.105064032A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2595T>A