Canonical Allele Identifier: CA2712886665
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs2114335285
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446566_126446567del , CM000668.2:g.126446566_126446567del GRCh38
NC_000006.11:g.126767712_126767713del , CM000668.1:g.126767712_126767713del GRCh37
NC_000006.10:g.126809405_126809406del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+25901_2417+25902del
ENST00000652383.1:n.630+85097_630+85098del
NR_104462.1:n.800+12941_800+12942del
NR_104462.2:n.474+12941_474+12942del
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