Canonical Allele Identifier: CA452990382

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470008A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148874A>T , CM000668.2:g.157148874A>T	GRCh38
NC_000006.11:g.157470008A>T , CM000668.1:g.157470008A>T	GRCh37
NC_000006.10:g.157511700A>T	NCBI36
NG_032093.1:g.375945A>T
NG_032093.2:g.375945A>T
NG_066624.1:g.377849A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3012A>T	ENSP00000055163.8:p.Pro1004=
ENST00000414678.8:c.2922A>T	ENSP00000412835.3:p.Pro974=
ENST00000637015.2:c.3012A>T	ENSP00000489729.2:p.Pro1004=
ENST00000319584.11:c.1026A>T	ENSP00000313006.7:p.Pro342=
ENST00000346085.10:c.3051A>T	ENSP00000344546.5:p.Pro1017=
ENST00000350026.10:c.2763A>T	ENSP00000055163.7:p.Pro921=
ENST00000414678.7:c.1170A>T	ENSP00000412835.2:p.Pro390=
ENST00000452544.2:n.913A>T
ENST00000635849.1:c.333A>T	ENSP00000490948.1:p.Pro111=
ENST00000636426.1:n.146A>T
ENST00000636930.2:c.3012A>T MANE Select	ENSP00000490491.2:p.Pro1004=
ENST00000637015.1:c.251A>T
ENST00000637568.1:c.55A>T
ENST00000637810.1:c.513A>T	ENSP00000489636.1:p.Pro171=
ENST00000637904.1:c.513A>T	ENSP00000490550.1:p.Pro171=
ENST00000647938.1:c.2802A>T	ENSP00000498155.1:p.Pro934=
ENST00000674190.1:n.1761A>T
ENST00000319584.10:c.1029A>T	ENSP00000313006.6:p.Pro343=
ENST00000346085.9:c.2802A>T	ENSP00000344546.4:p.Pro934=
ENST00000350026.9:c.2763A>T	ENSP00000055163.7:p.Pro921=
ENST00000414678.6:c.1170A>T	ENSP00000412835.2:p.Pro390=
ENST00000452544.1:n.859A>T
ENST00000478761.3:c.85A>T
NM_017519.2:c.2763A>T	NP_059989.2:p.Pro921=
NM_020732.3:c.2802A>T	NP_065783.3:p.Pro934=
XM_005267069.3:c.2763A>T	XP_005267126.2:p.Pro921=
XM_011535984.1:c.1713A>T	XP_011534286.1:p.Pro571=
XM_011535985.1:c.1533A>T	XP_011534287.1:p.Pro511=
XM_011535986.1:c.1293A>T	XP_011534288.1:p.Pro431=
XM_011535987.1:c.912A>T	XP_011534289.1:p.Pro304=
XM_011535988.1:c.-20+15667A>T	XP_011534290.1:n.-20+15667A>T
NM_001346813.1:c.2763A>T	NP_001333742.1:p.Pro921=
NM_001363725.1:c.513A>T	NP_001350654.1:p.Pro171=
XM_011535984.2:c.2844A>T	XP_011534286.2:p.Pro948=
XM_011535988.3:c.-20+15667A>T	XP_011534290.1:n.-20+15667A>T
XM_017011103.2:c.2844A>T	XP_016866592.1:p.Pro948=
XM_017011104.1:c.2844A>T	XP_016866593.1:p.Pro948=
XM_017011105.2:c.2844A>T	XP_016866594.1:p.Pro948=
XM_017011106.2:c.2844A>T	XP_016866595.1:p.Pro948=
XM_017011107.2:c.2664A>T	XP_016866596.1:p.Pro888=
XR_002956289.1:n.2927A>T
NM_001363725.2:c.513A>T	NP_001350654.1:p.Pro171=
NM_001371656.1:c.3051A>T	NP_001358585.1:p.Pro1017=
NM_001374820.1:c.3051A>T	NP_001361749.1:p.Pro1017=
NM_001374828.1:c.3012A>T MANE Select	NP_001361757.1:p.Pro1004=
NM_017519.3:c.3012A>T	NP_059989.3:p.Pro1004=