Canonical Allele Identifier: CA1675516989

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148713C= , CM000668.2:g.157148713C=	GRCh38
NC_000006.11:g.157469847C= , CM000668.1:g.157469847C=	GRCh37
NC_000006.10:g.157511539C=	NCBI36
NG_032093.1:g.375784C=
NG_032093.2:g.375784C=
NG_066624.1:g.377688C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2851C=	ENSP00000055163.8:p.Gln951=
ENST00000414678.8:c.2761C=	ENSP00000412835.3:p.Gln921=
ENST00000637015.2:c.2851C=	ENSP00000489729.2:p.Gln951=
ENST00000319584.11:c.865C=	ENSP00000313006.7:p.Gln289=
ENST00000346085.10:c.2890C=	ENSP00000344546.5:p.Gln964=
ENST00000350026.10:c.2602C=	ENSP00000055163.7:p.Gln868=
ENST00000414678.7:c.1009C=	ENSP00000412835.2:p.Gln337=
ENST00000452544.2:n.752C=
ENST00000635849.1:c.172C=	ENSP00000490948.1:p.Gln58=
ENST00000636930.2:c.2851C= MANE Select	ENSP00000490491.2:p.Gln951=
ENST00000637015.1:c.90C=
ENST00000637810.1:c.352C=	ENSP00000489636.1:p.Gln118=
ENST00000637904.1:c.352C=	ENSP00000490550.1:p.Gln118=
ENST00000647938.1:c.2641C=	ENSP00000498155.1:p.Gln881=
ENST00000674190.1:n.1600C=
ENST00000319584.10:c.868C=	ENSP00000313006.6:p.Gln290=
ENST00000346085.9:c.2641C=	ENSP00000344546.4:p.Gln881=
ENST00000350026.9:c.2602C=	ENSP00000055163.7:p.Gln868=
ENST00000414678.6:c.1009C=	ENSP00000412835.2:p.Gln337=
ENST00000452544.1:n.698C=
NM_017519.2:c.2602C=	NP_059989.2:p.Gln868=
NM_020732.3:c.2641C=	NP_065783.3:p.Gln881=
XM_005267069.3:c.2602C=	XP_005267126.2:p.Gln868=
XM_011535984.1:c.1552C=	XP_011534286.1:p.Gln518=
XM_011535985.1:c.1372C=	XP_011534287.1:p.Gln458=
XM_011535986.1:c.1132C=	XP_011534288.1:p.Gln378=
XM_011535987.1:c.751C=	XP_011534289.1:p.Gln251=
XM_011535988.1:c.-20+15506C=	XP_011534290.1:n.-20+15506C=
NM_001346813.1:c.2602C=	NP_001333742.1:p.Gln868=
NM_001363725.1:c.352C=	NP_001350654.1:p.Gln118=
XM_011535984.2:c.2683C=	XP_011534286.2:p.Gln895=
XM_011535988.3:c.-20+15506C=	XP_011534290.1:n.-20+15506C=
XM_017011103.2:c.2683C=	XP_016866592.1:p.Gln895=
XM_017011104.1:c.2683C=	XP_016866593.1:p.Gln895=
XM_017011105.2:c.2683C=	XP_016866594.1:p.Gln895=
XM_017011106.2:c.2683C=	XP_016866595.1:p.Gln895=
XM_017011107.2:c.2503C=	XP_016866596.1:p.Gln835=
XR_002956289.1:n.2766C=
NM_001363725.2:c.352C=	NP_001350654.1:p.Gln118=
NM_001371656.1:c.2890C=	NP_001358585.1:p.Gln964=
NM_001374820.1:c.2890C=	NP_001361749.1:p.Gln964=
NM_001374828.1:c.2851C= MANE Select	NP_001361757.1:p.Gln951=
NM_017519.3:c.2851C=	NP_059989.3:p.Gln951=