Canonical Allele Identifier: CA570432391
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs1348858381
gnomAD v2: 6-126767515-G-A
gnomAD v3: 6-126446369-G-A
gnomAD v4: 6-126446369-G-A
MyVariant Identifiers: chr6:g.126767515G>A (hg19) chr6:g.126446369G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446369G>A , CM000668.2:g.126446369G>A GRCh38
NC_000006.11:g.126767515G>A , CM000668.1:g.126767515G>A GRCh37
NC_000006.10:g.126809208G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+26098C>T
ENST00000652383.1:n.630+85294C>T
NR_104462.1:n.800+12744G>A
NR_104462.2:n.474+12744G>A
Search 100 bp 5'
Search 100 bp 3'