Canonical Allele Identifier: CA2772970028

Gene: CENPW

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.126446374A>C , CM000668.2:g.126446374A>C	GRCh38
NC_000006.11:g.126767520A>C , CM000668.1:g.126767520A>C	GRCh37
NC_000006.10:g.126809213A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651326.1:n.2417+26093T>G
ENST00000652383.1:n.630+85289T>G
NR_104462.1:n.800+12749A>C
NR_104462.2:n.474+12749A>C