Canonical Allele Identifier: CA1127548520

Gene: LINC01492

Linked Data

• dbSNP Id: rs1827343898
• gnomAD v3: 9-103262084-G-A
• gnomAD v4: 9-103262084-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103262084G>A , CM000671.2:g.103262084G>A	GRCh38
NC_000009.11:g.106024366G>A , CM000671.1:g.106024366G>A	GRCh37
NC_000009.10:g.105064187G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2440C>T