Canonical Allele Identifier: CA857924218
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1354074403

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262089A>C , CM000671.2:g.103262089A>C GRCh38
NC_000009.11:g.106024371A>C , CM000671.1:g.106024371A>C GRCh37
NC_000009.10:g.105064192A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2435T>G