Canonical Allele Identifier: CA1869205510
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827343530

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262050A>G , CM000671.2:g.103262050A>G GRCh38
NC_000009.11:g.106024332A>G , CM000671.1:g.106024332A>G GRCh37
NC_000009.10:g.105064153A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2474T>C