Canonical Allele Identifier: CA197961810
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs16922670

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261938T>C , CM000671.2:g.103261938T>C GRCh38
NC_000009.11:g.106024220T>C , CM000671.1:g.106024220T>C GRCh37
NC_000009.10:g.105064041T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2586A>G