Canonical Allele Identifier: CA366247147

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206695T>C , CM000668.2:g.157206695T>C	GRCh38
NC_000006.11:g.157527829T>C , CM000668.1:g.157527829T>C	GRCh37
NC_000006.10:g.157569521T>C	NCBI36
NG_032093.1:g.433766T>C
NG_032093.2:g.433766T>C
NG_066624.1:g.435670T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5764T>C	ENSP00000055163.8:p.Ser1922Pro
ENST00000414678.8:c.5833T>C	ENSP00000412835.3:p.Ser1945Pro
ENST00000637015.2:c.6052T>C	ENSP00000489729.2:p.Ser2018Pro
ENST00000346085.10:c.5803T>C	ENSP00000344546.5:p.Ser1935Pro
ENST00000350026.10:c.5515T>C	ENSP00000055163.7:p.Ser1839Pro
ENST00000414678.7:c.4081T>C	ENSP00000412835.2:p.Ser1361Pro
ENST00000635849.1:c.3244T>C	ENSP00000490948.1:p.Ser1082Pro
ENST00000635928.1:c.79T>C	ENSP00000489717.1:p.Ser27Pro
ENST00000635957.1:c.2875T>C	ENSP00000490385.1:p.Ser959Pro
ENST00000636227.1:n.4386T>C
ENST00000636254.1:n.1843T>C
ENST00000636930.2:c.5923T>C MANE Select	ENSP00000490491.2:p.Ser1975Pro
ENST00000636940.1:n.3920T>C
ENST00000637015.1:c.3291T>C
ENST00000637568.1:c.3205T>C
ENST00000637741.1:n.2589T>C
ENST00000637810.1:c.3265T>C	ENSP00000489636.1:p.Ser1089Pro
ENST00000637904.1:c.3424T>C	ENSP00000490550.1:p.Ser1142Pro
ENST00000637933.1:n.3038T>C
ENST00000647938.1:c.5554T>C	ENSP00000498155.1:p.Ser1852Pro
ENST00000346085.9:c.5554T>C	ENSP00000344546.4:p.Ser1852Pro
ENST00000350026.9:c.5515T>C	ENSP00000055163.7:p.Ser1839Pro
ENST00000414678.6:c.4081T>C	ENSP00000412835.2:p.Ser1361Pro
NM_017519.2:c.5515T>C	NP_059989.2:p.Ser1839Pro
NM_020732.3:c.5554T>C	NP_065783.3:p.Ser1852Pro
XM_005267069.3:c.5674T>C	XP_005267126.2:p.Ser1892Pro
XM_011535984.1:c.4753T>C	XP_011534286.1:p.Ser1585Pro
XM_011535985.1:c.4573T>C	XP_011534287.1:p.Ser1525Pro
XM_011535986.1:c.4333T>C	XP_011534288.1:p.Ser1445Pro
XM_011535987.1:c.3952T>C	XP_011534289.1:p.Ser1318Pro
XM_011535988.1:c.2815T>C	XP_011534290.1:p.Ser939Pro
NM_001346813.1:c.5674T>C	NP_001333742.1:p.Ser1892Pro
NM_001363725.1:c.3424T>C	NP_001350654.1:p.Ser1142Pro
XM_011535984.2:c.5884T>C	XP_011534286.2:p.Ser1962Pro
XM_011535988.3:c.2815T>C	XP_011534290.1:p.Ser939Pro
XM_017011103.2:c.5785T>C	XP_016866592.1:p.Ser1929Pro
XM_017011104.1:c.5755T>C	XP_016866593.1:p.Ser1919Pro
XM_017011105.2:c.5725T>C	XP_016866594.1:p.Ser1909Pro
XM_017011106.2:c.5596T>C	XP_016866595.1:p.Ser1866Pro
XM_017011107.2:c.5575T>C	XP_016866596.1:p.Ser1859Pro
XR_002956289.1:n.5870T>C
NM_001363725.2:c.3424T>C	NP_001350654.1:p.Ser1142Pro
NM_001371656.1:c.5803T>C	NP_001358585.1:p.Ser1935Pro
NM_001374820.1:c.5803T>C	NP_001361749.1:p.Ser1935Pro
NM_001374828.1:c.5923T>C MANE Select	NP_001361757.1:p.Ser1975Pro
NM_017519.3:c.5764T>C	NP_059989.3:p.Ser1922Pro