Canonical Allele Identifier: CA209938

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157167055C>T , CM000668.2:g.157167055C>T	GRCh38
NC_000006.11:g.157488189C>T , CM000668.1:g.157488189C>T	GRCh37
NC_000006.10:g.157529881C>T	NCBI36
NG_032093.1:g.394126C>T
NG_032093.2:g.394126C>T
NG_066624.1:g.396030C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.3105C>T MANE Select	NP_001361757.1:p.Pro1035=
ENST00000636930.2:c.3105C>T MANE Select	ENSP00000490491.2:p.Pro1035=
NM_001346813.1:c.2856C>T	NP_001333742.1:p.Pro952=
NM_001363725.1:c.606C>T	NP_001350654.1:p.Pro202=
NM_001363725.2:c.606C>T	NP_001350654.1:p.Pro202=
NM_001371656.1:c.3144C>T	NP_001358585.1:p.Pro1048=
NM_001374820.1:c.3144C>T	NP_001361749.1:p.Pro1048=
NM_017519.2:c.2856C>T	NP_059989.2:p.Pro952=
NM_017519.3:c.3105C>T	NP_059989.3:p.Pro1035=
NM_020732.3:c.2895C>T	NP_065783.3:p.Pro965=
ENST00000319584.10:c.1122C>T	ENSP00000313006.6:p.Pro374=
ENST00000319584.11:c.1119C>T	ENSP00000313006.7:p.Pro373=
ENST00000346085.10:c.3144C>T	ENSP00000344546.5:p.Pro1048=
ENST00000346085.9:c.2895C>T	ENSP00000344546.4:p.Pro965=
ENST00000350026.10:c.2856C>T	ENSP00000055163.7:p.Pro952=
ENST00000350026.11:c.3105C>T	ENSP00000055163.8:p.Pro1035=
ENST00000350026.9:c.2856C>T	ENSP00000055163.7:p.Pro952=
ENST00000400790.3:c.57C>T	ENSP00000383596.3:p.Pro19=
ENST00000414678.6:c.1263C>T	ENSP00000412835.2:p.Pro421=
ENST00000414678.7:c.1263C>T	ENSP00000412835.2:p.Pro421=
ENST00000414678.8:c.3015C>T	ENSP00000412835.3:p.Pro1005=
ENST00000478761.3:c.307C>T
ENST00000635849.1:c.426C>T	ENSP00000490948.1:p.Pro142=
ENST00000635957.1:c.60C>T	ENSP00000490385.1:p.Pro20=
ENST00000636426.1:n.269C>T
ENST00000637015.1:c.473C>T
ENST00000637015.2:c.3234C>T	ENSP00000489729.2:p.Pro1078=
ENST00000637568.1:c.387C>T
ENST00000637722.1:n.1041C>T
ENST00000637810.1:c.606C>T	ENSP00000489636.1:p.Pro202=
ENST00000637904.1:c.606C>T	ENSP00000490550.1:p.Pro202=
ENST00000647938.1:c.2895C>T	ENSP00000498155.1:p.Pro965=
XM_005267069.3:c.2856C>T	XP_005267126.2:p.Pro952=
XM_011535984.1:c.1935C>T	XP_011534286.1:p.Pro645=
XM_011535984.2:c.3066C>T	XP_011534286.2:p.Pro1022=
XM_011535985.1:c.1755C>T	XP_011534287.1:p.Pro585=
XM_011535986.1:c.1515C>T	XP_011534288.1:p.Pro505=
XM_011535987.1:c.1134C>T	XP_011534289.1:p.Pro378=
XM_011535988.1:c.-4C>T	XP_011534290.1:n.-4C>T
XM_011535988.3:c.-4C>T	XP_011534290.1:n.-4C>T
XM_017011103.2:c.2967C>T	XP_016866592.1:p.Pro989=
XM_017011104.1:c.2937C>T	XP_016866593.1:p.Pro979=
XM_017011105.2:c.3066C>T	XP_016866594.1:p.Pro1022=
XM_017011106.2:c.2937C>T	XP_016866595.1:p.Pro979=
XM_017011107.2:c.2757C>T	XP_016866596.1:p.Pro919=
XR_002956289.1:n.3149C>T