Canonical Allele Identifier: CA1094208478

Gene: CENPW

Linked Data

• gnomAD v3: 6-126446371-A-C
• gnomAD v4: 6-126446371-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.126446371A>C , CM000668.2:g.126446371A>C	GRCh38
NC_000006.11:g.126767517A>C , CM000668.1:g.126767517A>C	GRCh37
NC_000006.10:g.126809210A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651326.1:n.2417+26096T>G
ENST00000652383.1:n.630+85292T>G
NR_104462.1:n.800+12746A>C
NR_104462.2:n.474+12746A>C