Canonical Allele Identifier: CA962595885
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1883837848

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637444T>C , CM000676.2:g.44637444T>C GRCh38
NC_000014.8:g.45106647T>C , CM000676.1:g.45106647T>C GRCh37
NC_000014.7:g.44176397T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40431A>G
XR_943801.1:n.226-40431A>G
XR_943806.1:n.226-40431A>G
XR_943808.1:n.126+160486A>G