Canonical Allele Identifier: CA452978119

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522291T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201157T>G , CM000668.2:g.157201157T>G	GRCh38
NC_000006.11:g.157522291T>G , CM000668.1:g.157522291T>G	GRCh37
NC_000006.10:g.157563983T>G	NCBI36
NG_032093.1:g.428228T>G
NG_032093.2:g.428228T>G
NG_066624.1:g.430132T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4773T>G	ENSP00000055163.8:p.Pro1591=
ENST00000414678.8:c.4842T>G	ENSP00000412835.3:p.Pro1614=
ENST00000637015.2:c.5061T>G	ENSP00000489729.2:p.Pro1687=
ENST00000346085.10:c.4812T>G	ENSP00000344546.5:p.Pro1604=
ENST00000350026.10:c.4524T>G	ENSP00000055163.7:p.Pro1508=
ENST00000414678.7:c.3090T>G	ENSP00000412835.2:p.Pro1030=
ENST00000635849.1:c.2253T>G	ENSP00000490948.1:p.Pro751=
ENST00000635957.1:c.1884T>G	ENSP00000490385.1:p.Pro628=
ENST00000636227.1:n.3395T>G
ENST00000636254.1:n.852T>G
ENST00000636930.2:c.4932T>G MANE Select	ENSP00000490491.2:p.Pro1644=
ENST00000636940.1:n.2929T>G
ENST00000637015.1:c.2300T>G
ENST00000637568.1:c.2214T>G
ENST00000637741.1:n.1598T>G
ENST00000637810.1:c.2274T>G	ENSP00000489636.1:p.Pro758=
ENST00000637904.1:c.2433T>G	ENSP00000490550.1:p.Pro811=
ENST00000647938.1:c.4563T>G	ENSP00000498155.1:p.Pro1521=
ENST00000346085.9:c.4563T>G	ENSP00000344546.4:p.Pro1521=
ENST00000350026.9:c.4524T>G	ENSP00000055163.7:p.Pro1508=
ENST00000414678.6:c.3090T>G	ENSP00000412835.2:p.Pro1030=
NM_017519.2:c.4524T>G	NP_059989.2:p.Pro1508=
NM_020732.3:c.4563T>G	NP_065783.3:p.Pro1521=
XM_005267069.3:c.4683T>G	XP_005267126.2:p.Pro1561=
XM_011535984.1:c.3762T>G	XP_011534286.1:p.Pro1254=
XM_011535985.1:c.3582T>G	XP_011534287.1:p.Pro1194=
XM_011535986.1:c.3342T>G	XP_011534288.1:p.Pro1114=
XM_011535987.1:c.2961T>G	XP_011534289.1:p.Pro987=
XM_011535988.1:c.1824T>G	XP_011534290.1:p.Pro608=
NM_001346813.1:c.4683T>G	NP_001333742.1:p.Pro1561=
NM_001363725.1:c.2433T>G	NP_001350654.1:p.Pro811=
XM_011535984.2:c.4893T>G	XP_011534286.2:p.Pro1631=
XM_011535988.3:c.1824T>G	XP_011534290.1:p.Pro608=
XM_017011103.2:c.4794T>G	XP_016866592.1:p.Pro1598=
XM_017011104.1:c.4764T>G	XP_016866593.1:p.Pro1588=
XM_017011105.2:c.4734T>G	XP_016866594.1:p.Pro1578=
XM_017011106.2:c.4605T>G	XP_016866595.1:p.Pro1535=
XM_017011107.2:c.4584T>G	XP_016866596.1:p.Pro1528=
XR_002956289.1:n.4879T>G
NM_001363725.2:c.2433T>G	NP_001350654.1:p.Pro811=
NM_001371656.1:c.4812T>G	NP_001358585.1:p.Pro1604=
NM_001374820.1:c.4812T>G	NP_001361749.1:p.Pro1604=
NM_001374828.1:c.4932T>G MANE Select	NP_001361757.1:p.Pro1644=
NM_017519.3:c.4773T>G	NP_059989.3:p.Pro1591=