Canonical Allele Identifier: CA147692056
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs1361108
gnomAD v2: 6-126767600-C-T
gnomAD v3: 6-126446454-C-T
gnomAD v4: 6-126446454-C-T
MyVariant Identifiers: chr6:g.126767600C>T (hg19) chr6:g.126446454C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446454C>T , CM000668.2:g.126446454C>T GRCh38
NC_000006.11:g.126767600C>T , CM000668.1:g.126767600C>T GRCh37
NC_000006.10:g.126809293C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651326.1:n.2417+26013G>A
ENST00000652383.1:n.630+85209G>A
NR_104462.1:n.800+12829C>T
NR_104462.2:n.474+12829C>T
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