Canonical Allele Identifier: CA1675530447

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157174030G= , CM000668.2:g.157174030G=	GRCh38
NC_000006.11:g.157495164G= , CM000668.1:g.157495164G=	GRCh37
NC_000006.10:g.157536856G=	NCBI36
NG_032093.1:g.401101G=
NG_032093.2:g.401101G=
NG_066624.1:g.403005G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.3258G= MANE Select	NP_001361757.1:p.Met1086=
ENST00000636930.2:c.3258G= MANE Select	ENSP00000490491.2:p.Met1086=
NM_001346813.1:c.3009G=	NP_001333742.1:p.Met1003=
NM_001363725.1:c.759G=	NP_001350654.1:p.Met253=
NM_001363725.2:c.759G=	NP_001350654.1:p.Met253=
NM_001371656.1:c.3297G=	NP_001358585.1:p.Met1099=
NM_001374820.1:c.3297G=	NP_001361749.1:p.Met1099=
NM_017519.2:c.3009G=	NP_059989.2:p.Met1003=
NM_017519.3:c.3258G=	NP_059989.3:p.Met1086=
NM_020732.3:c.3048G=	NP_065783.3:p.Met1016=
ENST00000319584.10:c.1275G=	ENSP00000313006.6:p.Met425=
ENST00000319584.11:c.1272G=	ENSP00000313006.7:p.Met424=
ENST00000346085.10:c.3297G=	ENSP00000344546.5:p.Met1099=
ENST00000346085.9:c.3048G=	ENSP00000344546.4:p.Met1016=
ENST00000350026.10:c.3009G=	ENSP00000055163.7:p.Met1003=
ENST00000350026.11:c.3258G=	ENSP00000055163.8:p.Met1086=
ENST00000350026.9:c.3009G=	ENSP00000055163.7:p.Met1003=
ENST00000400790.3:c.210G=	ENSP00000383596.3:p.Met70=
ENST00000414678.6:c.1416G=	ENSP00000412835.2:p.Met472=
ENST00000414678.7:c.1416G=	ENSP00000412835.2:p.Met472=
ENST00000414678.8:c.3168G=	ENSP00000412835.3:p.Met1056=
ENST00000478761.3:c.460G=
ENST00000478761.4:n.46G=
ENST00000635849.1:c.579G=	ENSP00000490948.1:p.Met193=
ENST00000635957.1:c.213G=	ENSP00000490385.1:p.Met71=
ENST00000636940.1:n.1255G=
ENST00000637015.1:c.626G=
ENST00000637015.2:c.3387G=	ENSP00000489729.2:p.Met1129=
ENST00000637170.1:n.530G=
ENST00000637568.1:c.540G=
ENST00000637741.1:n.83G=
ENST00000637810.1:c.759G=	ENSP00000489636.1:p.Met253=
ENST00000637904.1:c.759G=	ENSP00000490550.1:p.Met253=
ENST00000647938.1:c.3048G=	ENSP00000498155.1:p.Met1016=
XM_005267069.3:c.3009G=	XP_005267126.2:p.Met1003=
XM_011535984.1:c.2088G=	XP_011534286.1:p.Met696=
XM_011535984.2:c.3219G=	XP_011534286.2:p.Met1073=
XM_011535985.1:c.1908G=	XP_011534287.1:p.Met636=
XM_011535986.1:c.1668G=	XP_011534288.1:p.Met556=
XM_011535987.1:c.1287G=	XP_011534289.1:p.Met429=
XM_011535988.1:c.150G=	XP_011534290.1:p.Met50=
XM_011535988.3:c.150G=	XP_011534290.1:p.Met50=
XM_017011103.2:c.3120G=	XP_016866592.1:p.Met1040=
XM_017011104.1:c.3090G=	XP_016866593.1:p.Met1030=
XM_017011105.2:c.3219G=	XP_016866594.1:p.Met1073=
XM_017011106.2:c.3090G=	XP_016866595.1:p.Met1030=
XM_017011107.2:c.2910G=	XP_016866596.1:p.Met970=
XR_002956289.1:n.3302G=