Canonical Allele Identifier: CA1127548525
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827344079

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262100A>G , CM000671.2:g.103262100A>G GRCh38
NC_000009.11:g.106024382A>G , CM000671.1:g.106024382A>G GRCh37
NC_000009.10:g.105064203A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2424T>C