Canonical Allele Identifier: CA2712886655
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs2114335047
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446364_126446365insCT , CM000668.2:g.126446364_126446365insCT GRCh38
NC_000006.11:g.126767510_126767511insCT , CM000668.1:g.126767510_126767511insCT GRCh37
NC_000006.10:g.126809203_126809204insCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+26102_2417+26103insAG
ENST00000652383.1:n.630+85298_630+85299insAG
NR_104462.1:n.800+12739_800+12740insCT
NR_104462.2:n.474+12739_474+12740insCT
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