Canonical Allele Identifier: CA1127548439

Gene: LINC01492

Linked Data

• dbSNP Id: rs1827340478
• gnomAD v3: 9-103261793-T-C
• gnomAD v4: 9-103261793-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261793T>C , CM000671.2:g.103261793T>C	GRCh38
NC_000009.11:g.106024075T>C , CM000671.1:g.106024075T>C	GRCh37
NC_000009.10:g.105063896T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2731A>G