Canonical Allele Identifier: CA570432422
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs1412585362
gnomAD v2: 6-126767711-T-C
gnomAD v3: 6-126446565-T-C
gnomAD v4: 6-126446565-T-C
MyVariant Identifiers: chr6:g.126767711T>C (hg19) chr6:g.126446565T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446565T>C , CM000668.2:g.126446565T>C GRCh38
NC_000006.11:g.126767711T>C , CM000668.1:g.126767711T>C GRCh37
NC_000006.10:g.126809404T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+25902A>G
ENST00000652383.1:n.630+85098A>G
NR_104462.1:n.800+12940T>C
NR_104462.2:n.474+12940T>C
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