Canonical Allele Identifier: CA1675517076

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148920A= , CM000668.2:g.157148920A=	GRCh38
NC_000006.11:g.157470054A= , CM000668.1:g.157470054A=	GRCh37
NC_000006.10:g.157511746A=	NCBI36
NG_032093.1:g.375991A=
NG_032093.2:g.375991A=
NG_066624.1:g.377895A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3058A=	ENSP00000055163.8:p.Met1020=
ENST00000414678.8:c.2968A=	ENSP00000412835.3:p.Met990=
ENST00000637015.2:c.3058A=	ENSP00000489729.2:p.Met1020=
ENST00000319584.11:c.1072A=	ENSP00000313006.7:p.Met358=
ENST00000346085.10:c.3097A=	ENSP00000344546.5:p.Met1033=
ENST00000350026.10:c.2809A=	ENSP00000055163.7:p.Met937=
ENST00000414678.7:c.1216A=	ENSP00000412835.2:p.Met406=
ENST00000452544.2:n.959A=
ENST00000635849.1:c.379A=	ENSP00000490948.1:p.Met127=
ENST00000635957.1:c.13A=	ENSP00000490385.1:p.Met5=
ENST00000636426.1:n.192A=
ENST00000636930.2:c.3058A= MANE Select	ENSP00000490491.2:p.Met1020=
ENST00000637015.1:c.297A=
ENST00000637568.1:c.101A=
ENST00000637810.1:c.559A=	ENSP00000489636.1:p.Met187=
ENST00000637904.1:c.559A=	ENSP00000490550.1:p.Met187=
ENST00000647938.1:c.2848A=	ENSP00000498155.1:p.Met950=
ENST00000674190.1:n.1807A=
ENST00000319584.10:c.1075A=	ENSP00000313006.6:p.Met359=
ENST00000346085.9:c.2848A=	ENSP00000344546.4:p.Met950=
ENST00000350026.9:c.2809A=	ENSP00000055163.7:p.Met937=
ENST00000400790.3:c.10A=	ENSP00000383596.3:p.Met4=
ENST00000414678.6:c.1216A=	ENSP00000412835.2:p.Met406=
ENST00000452544.1:n.905A=
ENST00000478761.3:c.131A=
NM_017519.2:c.2809A=	NP_059989.2:p.Met937=
NM_020732.3:c.2848A=	NP_065783.3:p.Met950=
XM_005267069.3:c.2809A=	XP_005267126.2:p.Met937=
XM_011535984.1:c.1759A=	XP_011534286.1:p.Met587=
XM_011535985.1:c.1579A=	XP_011534287.1:p.Met527=
XM_011535986.1:c.1339A=	XP_011534288.1:p.Met447=
XM_011535987.1:c.958A=	XP_011534289.1:p.Met320=
XM_011535988.1:c.-20+15713A=	XP_011534290.1:n.-20+15713A=
NM_001346813.1:c.2809A=	NP_001333742.1:p.Met937=
NM_001363725.1:c.559A=	NP_001350654.1:p.Met187=
XM_011535984.2:c.2890A=	XP_011534286.2:p.Met964=
XM_011535988.3:c.-20+15713A=	XP_011534290.1:n.-20+15713A=
XM_017011103.2:c.2890A=	XP_016866592.1:p.Met964=
XM_017011104.1:c.2890A=	XP_016866593.1:p.Met964=
XM_017011105.2:c.2890A=	XP_016866594.1:p.Met964=
XM_017011106.2:c.2890A=	XP_016866595.1:p.Met964=
XM_017011107.2:c.2710A=	XP_016866596.1:p.Met904=
XR_002956289.1:n.2973A=
NM_001363725.2:c.559A=	NP_001350654.1:p.Met187=
NM_001371656.1:c.3097A=	NP_001358585.1:p.Met1033=
NM_001374820.1:c.3097A=	NP_001361749.1:p.Met1033=
NM_001374828.1:c.3058A= MANE Select	NP_001361757.1:p.Met1020=
NM_017519.3:c.3058A=	NP_059989.3:p.Met1020=