Canonical Allele Identifier: CA8371333

Gene: AURKB

Linked Data

• dbSNP Id: rs1059476
• ExAC: 17:8108331 A / G
• gnomAD v2: 17-8108331-A-G
• gnomAD v3: 17-8205013-A-G
• gnomAD v4: 17-8205013-A-G
• MyVariant Identifiers: chr17:g.8108331A>G (hg19) ; chr17:g.8205013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8205013A>G , CM000679.2:g.8205013A>G	GRCh38
NC_000017.10:g.8108331A>G , CM000679.1:g.8108331A>G	GRCh37
NC_000017.9:g.8049056A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000585124.6:c.893T>C MANE Select	ENSP00000463999.1:p.Met298Thr
ENST00000316199.10:c.896T>C	ENSP00000313950.6:p.Met299Thr
ENST00000534871.5:c.770T>C	ENSP00000443869.1:p.Met257Thr
ENST00000578549.5:c.797T>C	ENSP00000462207.1:p.Met266Thr
ENST00000578753.1:n.415T>C
ENST00000580998.5:c.*240T>C	ENSP00000461981.1:n.*240T>C
ENST00000584972.5:c.585T>C
ENST00000585124.5:c.893T>C	ENSP00000463999.1:p.Met298Thr
NM_001256834.1:c.770T>C	NP_001243763.1:p.Met257Thr
NM_001256834.2:c.770T>C	NP_001243763.1:p.Met257Thr
NM_001284526.1:c.896T>C	NP_001271455.1:p.Met299Thr
NM_001313950.1:c.893T>C	NP_001300879.1:p.Met298Thr
NM_001313951.1:c.770T>C	NP_001300880.1:p.Met257Thr
NM_001313952.1:c.773T>C	NP_001300881.1:p.Met258Thr
NM_001313953.1:c.797T>C	NP_001300882.1:p.Met266Thr
NM_001313954.1:c.437T>C	NP_001300883.1:p.Met146Thr
NM_001313955.1:c.389T>C	NP_001300884.1:p.Met130Thr
NM_004217.3:c.893T>C	NP_004208.2:p.Met298Thr
NR_132730.1:n.873T>C
NR_132731.1:n.758T>C
XM_011524070.1:c.797T>C	XP_011522372.1:p.Met266Thr
XM_011524072.1:c.770T>C	XP_011522374.1:p.Met257Thr
XR_934118.1:n.1102T>C
NM_001313953.2:c.797T>C	NP_001300882.1:p.Met266Thr
XM_011524072.3:c.770T>C	XP_011522374.1:p.Met257Thr
XM_017025307.2:c.770T>C	XP_016880796.1:p.Met257Thr
XM_017025308.2:c.674T>C	XP_016880797.1:p.Met225Thr
XM_017025309.1:c.437T>C	XP_016880798.1:p.Met146Thr
XM_017025310.1:c.437T>C	XP_016880799.1:p.Met146Thr
XM_017025311.1:c.437T>C	XP_016880800.1:p.Met146Thr
NM_004217.4:c.893T>C MANE Select	NP_004208.2:p.Met298Thr
NM_001256834.3:c.770T>C	NP_001243763.1:p.Met257Thr
NM_001284526.2:c.896T>C	NP_001271455.1:p.Met299Thr
NM_001313950.2:c.893T>C	NP_001300879.1:p.Met298Thr
NM_001313952.2:c.773T>C	NP_001300881.1:p.Met258Thr
NM_001313953.3:c.797T>C	NP_001300882.1:p.Met266Thr
NM_001313954.2:c.437T>C	NP_001300883.1:p.Met146Thr
NM_001313955.2:c.389T>C	NP_001300884.1:p.Met130Thr
NR_132730.2:n.822T>C