Canonical Allele Identifier: CA197961824
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs149836294

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262010T>G , CM000671.2:g.103262010T>G GRCh38
NC_000009.11:g.106024292T>G , CM000671.1:g.106024292T>G GRCh37
NC_000009.10:g.105064113T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2514A>C