Canonical Allele Identifier: CA197961826
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs78467161

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262011G>A , CM000671.2:g.103262011G>A GRCh38
NC_000009.11:g.106024293G>A , CM000671.1:g.106024293G>A GRCh37
NC_000009.10:g.105064114G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2513C>T