Canonical Allele Identifier: CA197961818
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs961980562
MyVariant Identifiers: chr9:g.103261973C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261973C>G , CM000671.2:g.103261973C>G GRCh38
NC_000009.11:g.106024255C>G , CM000671.1:g.106024255C>G GRCh37
NC_000009.10:g.105064076C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2551G>C