Canonical Allele Identifier: CA452978411

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522195T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201061T>A , CM000668.2:g.157201061T>A	GRCh38
NC_000006.11:g.157522195T>A , CM000668.1:g.157522195T>A	GRCh37
NC_000006.10:g.157563887T>A	NCBI36
NG_032093.1:g.428132T>A
NG_032093.2:g.428132T>A
NG_066624.1:g.430036T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4677T>A	ENSP00000055163.8:p.Pro1559=
ENST00000414678.8:c.4746T>A	ENSP00000412835.3:p.Pro1582=
ENST00000637015.2:c.4965T>A	ENSP00000489729.2:p.Pro1655=
ENST00000346085.10:c.4716T>A	ENSP00000344546.5:p.Pro1572=
ENST00000350026.10:c.4428T>A	ENSP00000055163.7:p.Pro1476=
ENST00000414678.7:c.2994T>A	ENSP00000412835.2:p.Pro998=
ENST00000635849.1:c.2157T>A	ENSP00000490948.1:p.Pro719=
ENST00000635957.1:c.1788T>A	ENSP00000490385.1:p.Pro596=
ENST00000636227.1:n.3299T>A
ENST00000636254.1:n.756T>A
ENST00000636930.2:c.4836T>A MANE Select	ENSP00000490491.2:p.Pro1612=
ENST00000636940.1:n.2833T>A
ENST00000637015.1:c.2204T>A
ENST00000637568.1:c.2118T>A
ENST00000637741.1:n.1502T>A
ENST00000637810.1:c.2178T>A	ENSP00000489636.1:p.Pro726=
ENST00000637904.1:c.2337T>A	ENSP00000490550.1:p.Pro779=
ENST00000647938.1:c.4467T>A	ENSP00000498155.1:p.Pro1489=
ENST00000346085.9:c.4467T>A	ENSP00000344546.4:p.Pro1489=
ENST00000350026.9:c.4428T>A	ENSP00000055163.7:p.Pro1476=
ENST00000414678.6:c.2994T>A	ENSP00000412835.2:p.Pro998=
NM_017519.2:c.4428T>A	NP_059989.2:p.Pro1476=
NM_020732.3:c.4467T>A	NP_065783.3:p.Pro1489=
XM_005267069.3:c.4587T>A	XP_005267126.2:p.Pro1529=
XM_011535984.1:c.3666T>A	XP_011534286.1:p.Pro1222=
XM_011535985.1:c.3486T>A	XP_011534287.1:p.Pro1162=
XM_011535986.1:c.3246T>A	XP_011534288.1:p.Pro1082=
XM_011535987.1:c.2865T>A	XP_011534289.1:p.Pro955=
XM_011535988.1:c.1728T>A	XP_011534290.1:p.Pro576=
NM_001346813.1:c.4587T>A	NP_001333742.1:p.Pro1529=
NM_001363725.1:c.2337T>A	NP_001350654.1:p.Pro779=
XM_011535984.2:c.4797T>A	XP_011534286.2:p.Pro1599=
XM_011535988.3:c.1728T>A	XP_011534290.1:p.Pro576=
XM_017011103.2:c.4698T>A	XP_016866592.1:p.Pro1566=
XM_017011104.1:c.4668T>A	XP_016866593.1:p.Pro1556=
XM_017011105.2:c.4638T>A	XP_016866594.1:p.Pro1546=
XM_017011106.2:c.4509T>A	XP_016866595.1:p.Pro1503=
XM_017011107.2:c.4488T>A	XP_016866596.1:p.Pro1496=
XR_002956289.1:n.4783T>A
NM_001363725.2:c.2337T>A	NP_001350654.1:p.Pro779=
NM_001371656.1:c.4716T>A	NP_001358585.1:p.Pro1572=
NM_001374820.1:c.4716T>A	NP_001361749.1:p.Pro1572=
NM_001374828.1:c.4836T>A MANE Select	NP_001361757.1:p.Pro1612=
NM_017519.3:c.4677T>A	NP_059989.3:p.Pro1559=