Canonical Allele Identifier: CA1661800326
Gene: CENPW HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446562A= , CM000668.2:g.126446562A= GRCh38
NC_000006.11:g.126767708A= , CM000668.1:g.126767708A= GRCh37
NC_000006.10:g.126809401A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+25905T=
ENST00000652383.1:n.630+85101T=
NR_104462.1:n.800+12937A=
NR_104462.2:n.474+12937A=