Canonical Allele Identifier: CA147692065
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs1038682427
MyVariant Identifiers: chr6:g.126767706G>T (hg19) chr6:g.126446560G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446560G>T , CM000668.2:g.126446560G>T GRCh38
NC_000006.11:g.126767706G>T , CM000668.1:g.126767706G>T GRCh37
NC_000006.10:g.126809399G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+25907C>A
ENST00000652383.1:n.630+85103C>A
NR_104462.1:n.800+12935G>T
NR_104462.2:n.474+12935G>T
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