Canonical Allele Identifier: CA633983998

Gene: AURKC

Linked Data

• dbSNP Id: rs1218173282
• gnomAD v2: 19-57742476-G-T
• gnomAD v4: 19-57231108-G-T
• MyVariant Identifiers: chr19:g.57742476G>T (hg19) ; chr19:g.57231108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231108G>T , CM000681.2:g.57231108G>T	GRCh38
NC_000019.9:g.57742476G>T , CM000681.1:g.57742476G>T	GRCh37
NC_000019.8:g.62434288G>T	NCBI36
NG_012134.1:g.5100G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-141G>T MANE Select	ENSP00000302898.6:n.-141G>T
ENST00000302804.11:c.-141G>T	ENSP00000302898.6:n.-141G>T
ENST00000415300.6:c.-6G>T	ENSP00000407162.1:n.-6G>T
ENST00000448930.5:c.-57G>T	ENSP00000406798.2:n.-57G>T
NM_001015878.1:c.-141G>T	NP_001015878.1:n.-141G>T
NM_001015879.1:c.-6G>T	NP_001015879.1:n.-6G>T
NM_003160.2:c.-56G>T	NP_003151.2:n.-56G>T
XR_430209.2:n.749G>T
XR_430209.3:n.792G>T
NM_001015878.2:c.-141G>T MANE Select	NP_001015878.1:n.-141G>T
NM_001015879.2:c.-6G>T	NP_001015879.1:n.-6G>T
NM_003160.3:c.-56G>T	NP_003151.2:n.-56G>T