Canonical Allele Identifier: CA1869205499
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1587822223

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262032A>G , CM000671.2:g.103262032A>G GRCh38
NC_000009.11:g.106024314A>G , CM000671.1:g.106024314A>G GRCh37
NC_000009.10:g.105064135A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2492T>C