Canonical Allele Identifier: CA286588526
Gene: CDK10 HGNC NCBI

Linked Data

dbSNP Id: rs554654572
gnomAD v3: 16-89675091-G-A
gnomAD v4: 16-89675091-G-A
MyVariant Identifiers: chr16:g.89741499G>A (hg19) chr16:g.89675091G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89675091G>A , CM000678.2:g.89675091G>A GRCh38
NC_000016.9:g.89741499G>A , CM000678.1:g.89741499G>A GRCh37
NC_000016.8:g.88269000G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011523409.1:c.-1092+1798G>A XP_011521711.1:n.-1092+1798G>A
XM_011523418.1:c.-1092+1798G>A XP_011521720.1:n.-1092+1798G>A
XR_933471.1:n.855+1798G>A
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