Canonical Allele Identifier: CA1127548518

Gene: LINC01492

Linked Data

• dbSNP Id: rs1827343703
• gnomAD v3: 9-103262065-C-A
• gnomAD v4: 9-103262065-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103262065C>A , CM000671.2:g.103262065C>A	GRCh38
NC_000009.11:g.106024347C>A , CM000671.1:g.106024347C>A	GRCh37
NC_000009.10:g.105064168C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2459G>T