Canonical Allele Identifier: CA2133363496

Gene: LINC02302

Linked Data

• dbSNP Id: rs1883836577

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637338C>G , CM000676.2:g.44637338C>G	GRCh38
NC_000014.8:g.45106541C>G , CM000676.1:g.45106541C>G	GRCh37
NC_000014.7:g.44176291C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40325G>C
XR_943801.1:n.226-40325G>C
XR_943806.1:n.226-40325G>C
XR_943808.1:n.126+160592G>C