Canonical Allele Identifier: CA818587625

Gene: CENPW

Linked Data

• dbSNP Id: rs1255193650
• MyVariant Identifiers: chr6:g.126767505_126767506insG (hg19) ; chr6:g.126446359_126446360insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.126446359_126446360insG , CM000668.2:g.126446359_126446360insG	GRCh38
NC_000006.11:g.126767505_126767506insG , CM000668.1:g.126767505_126767506insG	GRCh37
NC_000006.10:g.126809198_126809199insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651326.1:n.2417+26107_2417+26108insC
ENST00000652383.1:n.630+85303_630+85304insC
NR_104462.1:n.800+12734_800+12735insG
NR_104462.2:n.474+12734_474+12735insG