Canonical Allele Identifier: CA147692045
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs369522986
gnomAD v2: 6-126767510-CA-C
gnomAD v3: 6-126446364-CA-C
gnomAD v4: 6-126446364-CA-C
MyVariant Identifiers: chr6:g.126767511del (hg19) chr6:g.126446365del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446365del , CM000668.2:g.126446365del GRCh38
NC_000006.11:g.126767511del , CM000668.1:g.126767511del GRCh37
NC_000006.10:g.126809204del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+26102del
ENST00000652383.1:n.630+85298del
NR_104462.1:n.800+12740del
NR_104462.2:n.474+12740del
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