Canonical Allele Identifier: CA89646426
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs266717
MyVariant Identifiers: chr3:g.186812695T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812695T>G , CM000665.2:g.186812695T>G GRCh38
NC_000003.11:g.186530484T>G , CM000665.1:g.186530484T>G GRCh37
NC_000003.10:g.188013178T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-547A>C