Canonical Allele Identifier: CA818587789

Gene: CENPW

Linked Data

• dbSNP Id: rs1209791440
• MyVariant Identifiers: chr6:g.126767708A>C (hg19) ; chr6:g.126446562A>C (hg38)

Genomic Alleles

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

Transcript Alleles

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