Canonical Allele Identifier: CA548460177
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1477168810

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812657A>C , CM000665.2:g.186812657A>C GRCh38
NC_000003.11:g.186530446A>C , CM000665.1:g.186530446A>C GRCh37
NC_000003.10:g.188013140A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-509T>G