Canonical Allele Identifier: CA147692037
Gene: CENPW HGNC NCBI

Linked Data

dbSNP Id: rs541544976
gnomAD v2: 6-126767506-C-G
gnomAD v3: 6-126446360-C-G
gnomAD v4: 6-126446360-C-G
MyVariant Identifiers: chr6:g.126767506C>G (hg19) chr6:g.126446360C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126446360C>G , CM000668.2:g.126446360C>G GRCh38
NC_000006.11:g.126767506C>G , CM000668.1:g.126767506C>G GRCh37
NC_000006.10:g.126809199C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651326.1:n.2417+26107G>C
ENST00000652383.1:n.630+85303G>C
NR_104462.1:n.800+12735C>G
NR_104462.2:n.474+12735C>G
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