Canonical Allele Identifier: CA2133363500
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1883836697

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637349T>G , CM000676.2:g.44637349T>G GRCh38
NC_000014.8:g.45106552T>G , CM000676.1:g.45106552T>G GRCh37
NC_000014.7:g.44176302T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40336A>C
XR_943801.1:n.226-40336A>C
XR_943806.1:n.226-40336A>C
XR_943808.1:n.126+160581A>C