Canonical Allele Identifier: CA1869205535
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827344002

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262095T>G , CM000671.2:g.103262095T>G GRCh38
NC_000009.11:g.106024377T>G , CM000671.1:g.106024377T>G GRCh37
NC_000009.10:g.105064198T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2429A>C