Canonical Allele Identifier: CA2133363560
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1883838925

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637509_44637510del , CM000676.2:g.44637509_44637510del GRCh38
NC_000014.8:g.45106712_45106713del , CM000676.1:g.45106712_45106713del GRCh37
NC_000014.7:g.44176462_44176463del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40496_226-40495del
XR_943801.1:n.226-40496_226-40495del
XR_943806.1:n.226-40496_226-40495del
XR_943808.1:n.126+160421_126+160422del