Canonical Allele Identifier: CA310421669
Gene: AURKC HGNC NCBI

Linked Data

dbSNP Id: rs901083202
gnomAD v4: 19-57231026-C-A
MyVariant Identifiers: chr19:g.57231026C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231026C>A , CM000681.2:g.57231026C>A GRCh38
NC_000019.9:g.57742394C>A , CM000681.1:g.57742394C>A GRCh37
NC_000019.8:g.62434206C>A NCBI36
NG_012134.1:g.5018C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-223C>A MANE Select ENSP00000302898.6:n.-223C>A
ENST00000415300.6:c.-88C>A ENSP00000407162.1:n.-88C>A
ENST00000448930.5:c.-139C>A ENSP00000406798.2:n.-139C>A
NM_001015879.1:c.-88C>A NP_001015879.1:n.-88C>A
NM_003160.2:c.-138C>A NP_003151.2:n.-138C>A
XR_430209.2:n.667C>A
XR_430209.3:n.710C>A
NM_001015878.2:c.-223C>A MANE Select NP_001015878.1:n.-223C>A
NM_001015879.2:c.-88C>A NP_001015879.1:n.-88C>A
NM_003160.3:c.-138C>A NP_003151.2:n.-138C>A
Search 100 bp 5'
Search 100 bp 3'