Canonical Allele Identifier: CA197961836

Gene: LINC01492

Linked Data

• dbSNP Id: rs977612380
• gnomAD v3: 9-103262037-T-C
• gnomAD v4: 9-103262037-T-C
• MyVariant Identifiers: chr9:g.106024319T>C (hg19) ; chr9:g.103262037T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103262037T>C , CM000671.2:g.103262037T>C	GRCh38
NC_000009.11:g.106024319T>C , CM000671.1:g.106024319T>C	GRCh37
NC_000009.10:g.105064140T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2487A>G