Canonical Allele Identifier: CA997443085
Gene: AURKC HGNC NCBI

Linked Data

dbSNP Id: rs1599969189
gnomAD v3: 19-57231029-T-C
gnomAD v4: 19-57231029-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231029T>C , CM000681.2:g.57231029T>C GRCh38
NC_000019.9:g.57742397T>C , CM000681.1:g.57742397T>C GRCh37
NC_000019.8:g.62434209T>C NCBI36
NG_012134.1:g.5021T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-220T>C MANE Select ENSP00000302898.6:n.-220T>C
ENST00000415300.6:c.-85T>C ENSP00000407162.1:n.-85T>C
ENST00000448930.5:c.-136T>C ENSP00000406798.2:n.-136T>C
NM_001015879.1:c.-85T>C NP_001015879.1:n.-85T>C
NM_003160.2:c.-135T>C NP_003151.2:n.-135T>C
XR_430209.2:n.670T>C
XR_430209.3:n.713T>C
NM_001015878.2:c.-220T>C MANE Select NP_001015878.1:n.-220T>C
NM_001015879.2:c.-85T>C NP_001015879.1:n.-85T>C
NM_003160.3:c.-135T>C NP_003151.2:n.-135T>C
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