Canonical Allele Identifier: CA197961771

Gene: LINC01492

Linked Data

• dbSNP Id: rs535789191
• gnomAD v3: 9-103261801-T-C
• gnomAD v4: 9-103261801-T-C
• MyVariant Identifiers: chr9:g.106024083T>C (hg19) ; chr9:g.103261801T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261801T>C , CM000671.2:g.103261801T>C	GRCh38
NC_000009.11:g.106024083T>C , CM000671.1:g.106024083T>C	GRCh37
NC_000009.10:g.105063904T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2723A>G