Canonical Allele Identifier: CA16043614

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157203997G>A , CM000668.2:g.157203997G>A	GRCh38
NC_000006.11:g.157525131G>A , CM000668.1:g.157525131G>A	GRCh37
NC_000006.10:g.157566823G>A	NCBI36
NG_032093.1:g.431068G>A
NG_032093.2:g.431068G>A
NG_066624.1:g.432972G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5235+1G>A	ENSP00000055163.8:n.5235+1G>A
ENST00000414678.8:c.5304+1G>A	ENSP00000412835.3:n.5304+1G>A
ENST00000637015.2:c.5523+1G>A	ENSP00000489729.2:n.5523+1G>A
ENST00000346085.10:c.5274+1G>A	ENSP00000344546.5:n.5274+1G>A
ENST00000350026.10:c.4986+1G>A	ENSP00000055163.7:n.4986+1G>A
ENST00000414678.7:c.3552+1G>A	ENSP00000412835.2:n.3552+1G>A
ENST00000635849.1:c.2715+1G>A	ENSP00000490948.1:n.2715+1G>A
ENST00000635957.1:c.2346+1G>A	ENSP00000490385.1:n.2346+1G>A
ENST00000636227.1:n.3857+1G>A
ENST00000636254.1:n.1314+1G>A
ENST00000636930.2:c.5394+1G>A MANE Select	ENSP00000490491.2:n.5394+1G>A
ENST00000636940.1:n.3391+1G>A
ENST00000637015.1:c.2762+1G>A
ENST00000637568.1:c.2676+1G>A
ENST00000637741.1:n.2060+1G>A
ENST00000637810.1:c.2736+1G>A	ENSP00000489636.1:n.2736+1G>A
ENST00000637904.1:c.2895+1G>A	ENSP00000490550.1:n.2895+1G>A
ENST00000637933.1:n.340G>A
ENST00000647938.1:c.5025+1G>A	ENSP00000498155.1:n.5025+1G>A
ENST00000346085.9:c.5025+1G>A	ENSP00000344546.4:n.5025+1G>A
ENST00000350026.9:c.4986+1G>A	ENSP00000055163.7:n.4986+1G>A
ENST00000414678.6:c.3552+1G>A	ENSP00000412835.2:n.3552+1G>A
NM_017519.2:c.4986+1G>A	NP_059989.2:n.4986+1G>A
NM_020732.3:c.5025+1G>A	NP_065783.3:n.5025+1G>A
XM_005267069.3:c.5145+1G>A	XP_005267126.2:n.5145+1G>A
XM_011535984.1:c.4224+1G>A	XP_011534286.1:n.4224+1G>A
XM_011535985.1:c.4044+1G>A	XP_011534287.1:n.4044+1G>A
XM_011535986.1:c.3804+1G>A	XP_011534288.1:n.3804+1G>A
XM_011535987.1:c.3423+1G>A	XP_011534289.1:n.3423+1G>A
XM_011535988.1:c.2286+1G>A	XP_011534290.1:n.2286+1G>A
NM_001346813.1:c.5145+1G>A	NP_001333742.1:n.5145+1G>A
NM_001363725.1:c.2895+1G>A	NP_001350654.1:n.2895+1G>A
XM_011535984.2:c.5355+1G>A	XP_011534286.2:n.5355+1G>A
XM_011535988.3:c.2286+1G>A	XP_011534290.1:n.2286+1G>A
XM_017011103.2:c.5256+1G>A	XP_016866592.1:n.5256+1G>A
XM_017011104.1:c.5226+1G>A	XP_016866593.1:n.5226+1G>A
XM_017011105.2:c.5196+1G>A	XP_016866594.1:n.5196+1G>A
XM_017011106.2:c.5067+1G>A	XP_016866595.1:n.5067+1G>A
XM_017011107.2:c.5046+1G>A	XP_016866596.1:n.5046+1G>A
XR_002956289.1:n.5341+1G>A
NM_001363725.2:c.2895+1G>A	NP_001350654.1:n.2895+1G>A
NM_001371656.1:c.5274+1G>A	NP_001358585.1:n.5274+1G>A
NM_001374820.1:c.5274+1G>A	NP_001361749.1:n.5274+1G>A
NM_001374828.1:c.5394+1G>A MANE Select	NP_001361757.1:n.5394+1G>A
NM_017519.3:c.5235+1G>A	NP_059989.3:n.5235+1G>A