Canonical Allele Identifier: CA147692040
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs768616549
gnomAD v2: 6-126767509-C-A
gnomAD v3: 6-126446363-C-A
gnomAD v4: 6-126446363-C-A
MyVariant Identifiers: chr6:g.126767509C>A (hg19) chr6:g.126767509_126767511delinsACA (hg19) chr6:g.126446363C>A (hg38) chr6:g.126446363_126446365delinsACA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446363C>A , CM000668.2:g.126446363C>A GRCh38
NC_000006.11:g.126767509C>A , CM000668.1:g.126767509C>A GRCh37
NC_000006.10:g.126809202C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+26104G>T
ENST00000652383.1:n.630+85300G>T
NR_104462.1:n.800+12738C>A
NR_104462.2:n.474+12738C>A
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