Canonical Allele Identifier: CA197961776

Gene: LINC01492

Linked Data

• dbSNP Id: rs760603803
• gnomAD v2: 9-106024112-G-A
• gnomAD v3: 9-103261830-G-A
• gnomAD v4: 9-103261830-G-A
• MyVariant Identifiers: chr9:g.106024112G>A (hg19) ; chr9:g.103261830G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261830G>A , CM000671.2:g.103261830G>A	GRCh38
NC_000009.11:g.106024112G>A , CM000671.1:g.106024112G>A	GRCh37
NC_000009.10:g.105063933G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2694C>T