Canonical Allele Identifier: CA2635977181

Gene: AURKB

Linked Data

• gnomAD v4: 17-8204733-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204733A>C , CM000679.2:g.8204733A>C	GRCh38
NC_000017.10:g.8108051A>C , CM000679.1:g.8108051A>C	GRCh37
NC_000017.9:g.8048776A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316199.10:c.*138T>G	ENSP00000313950.6:n.*138T>G
NM_001256834.1:c.*138T>G	NP_001243763.1:n.*138T>G
NM_001256834.2:c.*138T>G	NP_001243763.1:n.*138T>G
NM_001284526.1:c.*138T>G	NP_001271455.1:n.*138T>G
NM_001313950.1:c.*138T>G	NP_001300879.1:n.*138T>G
NM_001313951.1:c.*138T>G	NP_001300880.1:n.*138T>G
NM_001313952.1:c.*138T>G	NP_001300881.1:n.*138T>G
NM_001313953.1:c.*138T>G	NP_001300882.1:n.*138T>G
NM_001313954.1:c.*138T>G	NP_001300883.1:n.*138T>G
NM_001313955.1:c.*138T>G	NP_001300884.1:n.*138T>G
NM_004217.3:c.*138T>G	NP_004208.2:n.*138T>G
NR_132730.1:n.1153T>G
NR_132731.1:n.1038T>G
NM_001313953.2:c.*138T>G	NP_001300882.1:n.*138T>G