Canonical Allele Identifier: CA818587609

Gene: CENPW

Linked Data

• dbSNP Id: rs1364569564
• gnomAD v3: 6-126446357-G-C
• gnomAD v4: 6-126446357-G-C
• MyVariant Identifiers: chr6:g.126767503G>C (hg19) ; chr6:g.126446357G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.126446357G>C , CM000668.2:g.126446357G>C	GRCh38
NC_000006.11:g.126767503G>C , CM000668.1:g.126767503G>C	GRCh37
NC_000006.10:g.126809196G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651326.1:n.2417+26110C>G
ENST00000652383.1:n.630+85306C>G
NR_104462.1:n.800+12732G>C
NR_104462.2:n.474+12732G>C