Canonical Allele Identifier: CA310421678

Gene: AURKC

Linked Data

• dbSNP Id: rs567265006
• gnomAD v3: 19-57231033-T-C
• gnomAD v4: 19-57231033-T-C
• MyVariant Identifiers: chr19:g.57742401T>C (hg19) ; chr19:g.57231033T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231033T>C , CM000681.2:g.57231033T>C	GRCh38
NC_000019.9:g.57742401T>C , CM000681.1:g.57742401T>C	GRCh37
NC_000019.8:g.62434213T>C	NCBI36
NG_012134.1:g.5025T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-216T>C MANE Select	ENSP00000302898.6:n.-216T>C
ENST00000415300.6:c.-81T>C	ENSP00000407162.1:n.-81T>C
ENST00000448930.5:c.-132T>C	ENSP00000406798.2:n.-132T>C
NM_001015879.1:c.-81T>C	NP_001015879.1:n.-81T>C
NM_003160.2:c.-131T>C	NP_003151.2:n.-131T>C
XR_430209.2:n.674T>C
XR_430209.3:n.717T>C
NM_001015878.2:c.-216T>C MANE Select	NP_001015878.1:n.-216T>C
NM_001015879.2:c.-81T>C	NP_001015879.1:n.-81T>C
NM_003160.3:c.-131T>C	NP_003151.2:n.-131T>C