Canonical Allele Identifier: CA725760281
Gene: CDK10 HGNC NCBI

Linked Data

dbSNP Id: rs1232918983
MyVariant Identifiers: chr16:g.89741512A>T (hg19) chr16:g.89675104A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89675104A>T , CM000678.2:g.89675104A>T GRCh38
NC_000016.9:g.89741512A>T , CM000678.1:g.89741512A>T GRCh37
NC_000016.8:g.88269013A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011523409.1:c.-1092+1811A>T XP_011521711.1:n.-1092+1811A>T
XM_011523418.1:c.-1092+1811A>T XP_011521720.1:n.-1092+1811A>T
XR_933471.1:n.855+1811A>T
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