Canonical Allele Identifier: CA1869205538
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827344053

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262098G>A , CM000671.2:g.103262098G>A GRCh38
NC_000009.11:g.106024380G>A , CM000671.1:g.106024380G>A GRCh37
NC_000009.10:g.105064201G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2426C>T