Canonical Allele Identifier: CA147692064
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs944393539
MyVariant Identifiers: chr6:g.126767705A>G (hg19) chr6:g.126446559A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446559A>G , CM000668.2:g.126446559A>G GRCh38
NC_000006.11:g.126767705A>G , CM000668.1:g.126767705A>G GRCh37
NC_000006.10:g.126809398A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+25908T>C
ENST00000652383.1:n.630+85104T>C
NR_104462.1:n.800+12934A>G
NR_104462.2:n.474+12934A>G
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