Canonical Allele Identifier: CA366246283

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206407G>T , CM000668.2:g.157206407G>T	GRCh38
NC_000006.11:g.157527541G>T , CM000668.1:g.157527541G>T	GRCh37
NC_000006.10:g.157569233G>T	NCBI36
NG_032093.1:g.433478G>T
NG_032093.2:g.433478G>T
NG_066624.1:g.435382G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5635G>T MANE Select	NP_001361757.1:p.Glu1879Ter
ENST00000636930.2:c.5635G>T MANE Select	ENSP00000490491.2:p.Glu1879Ter
NM_001346813.1:c.5386G>T	NP_001333742.1:p.Glu1796Ter
NM_001363725.1:c.3136G>T	NP_001350654.1:p.Glu1046Ter
NM_001363725.2:c.3136G>T	NP_001350654.1:p.Glu1046Ter
NM_001371656.1:c.5515G>T	NP_001358585.1:p.Glu1839Ter
NM_001374820.1:c.5515G>T	NP_001361749.1:p.Glu1839Ter
NM_017519.2:c.5227G>T	NP_059989.2:p.Glu1743Ter
NM_017519.3:c.5476G>T	NP_059989.3:p.Glu1826Ter
NM_020732.3:c.5266G>T	NP_065783.3:p.Glu1756Ter
ENST00000346085.10:c.5515G>T	ENSP00000344546.5:p.Glu1839Ter
ENST00000346085.9:c.5266G>T	ENSP00000344546.4:p.Glu1756Ter
ENST00000350026.10:c.5227G>T	ENSP00000055163.7:p.Glu1743Ter
ENST00000350026.11:c.5476G>T	ENSP00000055163.8:p.Glu1826Ter
ENST00000350026.9:c.5227G>T	ENSP00000055163.7:p.Glu1743Ter
ENST00000414678.6:c.3793G>T	ENSP00000412835.2:p.Glu1265Ter
ENST00000414678.7:c.3793G>T	ENSP00000412835.2:p.Glu1265Ter
ENST00000414678.8:c.5545G>T	ENSP00000412835.3:p.Glu1849Ter
ENST00000635849.1:c.2956G>T	ENSP00000490948.1:p.Glu986Ter
ENST00000635957.1:c.2587G>T	ENSP00000490385.1:p.Glu863Ter
ENST00000636227.1:n.4098G>T
ENST00000636254.1:n.1555G>T
ENST00000636940.1:n.3632G>T
ENST00000637015.1:c.3003G>T
ENST00000637015.2:c.5764G>T	ENSP00000489729.2:p.Glu1922Ter
ENST00000637568.1:c.2917G>T
ENST00000637741.1:n.2301G>T
ENST00000637810.1:c.2977G>T	ENSP00000489636.1:p.Glu993Ter
ENST00000637904.1:c.3136G>T	ENSP00000490550.1:p.Glu1046Ter
ENST00000637933.1:n.2750G>T
ENST00000647938.1:c.5266G>T	ENSP00000498155.1:p.Glu1756Ter
XM_005267069.3:c.5386G>T	XP_005267126.2:p.Glu1796Ter
XM_011535984.1:c.4465G>T	XP_011534286.1:p.Glu1489Ter
XM_011535984.2:c.5596G>T	XP_011534286.2:p.Glu1866Ter
XM_011535985.1:c.4285G>T	XP_011534287.1:p.Glu1429Ter
XM_011535986.1:c.4045G>T	XP_011534288.1:p.Glu1349Ter
XM_011535987.1:c.3664G>T	XP_011534289.1:p.Glu1222Ter
XM_011535988.1:c.2527G>T	XP_011534290.1:p.Glu843Ter
XM_011535988.3:c.2527G>T	XP_011534290.1:p.Glu843Ter
XM_017011103.2:c.5497G>T	XP_016866592.1:p.Glu1833Ter
XM_017011104.1:c.5467G>T	XP_016866593.1:p.Glu1823Ter
XM_017011105.2:c.5437G>T	XP_016866594.1:p.Glu1813Ter
XM_017011106.2:c.5308G>T	XP_016866595.1:p.Glu1770Ter
XM_017011107.2:c.5287G>T	XP_016866596.1:p.Glu1763Ter
XR_002956289.1:n.5582G>T