Canonical Allele Identifier: CA570432412
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs1204800437
gnomAD v2: 6-126767629-T-G
gnomAD v3: 6-126446483-T-G
gnomAD v4: 6-126446483-T-G
MyVariant Identifiers: chr6:g.126767629T>G (hg19) chr6:g.126446483T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446483T>G , CM000668.2:g.126446483T>G GRCh38
NC_000006.11:g.126767629T>G , CM000668.1:g.126767629T>G GRCh37
NC_000006.10:g.126809322T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+25984A>C
ENST00000652383.1:n.630+85180A>C
NR_104462.1:n.800+12858T>G
NR_104462.2:n.474+12858T>G
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