Canonical Allele Identifier: CA197961804

Gene: LINC01492

Linked Data

• dbSNP Id: rs957523180
• gnomAD v3: 9-103261931-T-C
• gnomAD v4: 9-103261931-T-C
• MyVariant Identifiers: chr9:g.106024213T>C (hg19) ; chr9:g.103261931T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261931T>C , CM000671.2:g.103261931T>C	GRCh38
NC_000009.11:g.106024213T>C , CM000671.1:g.106024213T>C	GRCh37
NC_000009.10:g.105064034T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2593A>G