Canonical Allele Identifier: CA857924216
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1441367150

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262079C>T , CM000671.2:g.103262079C>T GRCh38
NC_000009.11:g.106024361C>T , CM000671.1:g.106024361C>T GRCh37
NC_000009.10:g.105064182C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2445G>A