Canonical Allele Identifier: CA2504817991
Gene: CENPW HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446462G>C , CM000668.2:g.126446462G>C GRCh38
NC_000006.11:g.126767608G>C , CM000668.1:g.126767608G>C GRCh37
NC_000006.10:g.126809301G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+26005C>G
ENST00000652383.1:n.630+85201C>G
NR_104462.1:n.800+12837G>C
NR_104462.2:n.474+12837G>C