Canonical Allele Identifier: CA366241963

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522228G>A (hg19) ; chr6:g.157201094G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201094G>A , CM000668.2:g.157201094G>A	GRCh38
NC_000006.11:g.157522228G>A , CM000668.1:g.157522228G>A	GRCh37
NC_000006.10:g.157563920G>A	NCBI36
NG_032093.1:g.428165G>A
NG_032093.2:g.428165G>A
NG_066624.1:g.430069G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4710G>A	ENSP00000055163.8:p.Met1570Ile
ENST00000414678.8:c.4779G>A	ENSP00000412835.3:p.Met1593Ile
ENST00000637015.2:c.4998G>A	ENSP00000489729.2:p.Met1666Ile
ENST00000346085.10:c.4749G>A	ENSP00000344546.5:p.Met1583Ile
ENST00000350026.10:c.4461G>A	ENSP00000055163.7:p.Met1487Ile
ENST00000414678.7:c.3027G>A	ENSP00000412835.2:p.Met1009Ile
ENST00000635849.1:c.2190G>A	ENSP00000490948.1:p.Met730Ile
ENST00000635957.1:c.1821G>A	ENSP00000490385.1:p.Met607Ile
ENST00000636227.1:n.3332G>A
ENST00000636254.1:n.789G>A
ENST00000636930.2:c.4869G>A MANE Select	ENSP00000490491.2:p.Met1623Ile
ENST00000636940.1:n.2866G>A
ENST00000637015.1:c.2237G>A
ENST00000637568.1:c.2151G>A
ENST00000637741.1:n.1535G>A
ENST00000637810.1:c.2211G>A	ENSP00000489636.1:p.Met737Ile
ENST00000637904.1:c.2370G>A	ENSP00000490550.1:p.Met790Ile
ENST00000647938.1:c.4500G>A	ENSP00000498155.1:p.Met1500Ile
ENST00000346085.9:c.4500G>A	ENSP00000344546.4:p.Met1500Ile
ENST00000350026.9:c.4461G>A	ENSP00000055163.7:p.Met1487Ile
ENST00000414678.6:c.3027G>A	ENSP00000412835.2:p.Met1009Ile
NM_017519.2:c.4461G>A	NP_059989.2:p.Met1487Ile
NM_020732.3:c.4500G>A	NP_065783.3:p.Met1500Ile
XM_005267069.3:c.4620G>A	XP_005267126.2:p.Met1540Ile
XM_011535984.1:c.3699G>A	XP_011534286.1:p.Met1233Ile
XM_011535985.1:c.3519G>A	XP_011534287.1:p.Met1173Ile
XM_011535986.1:c.3279G>A	XP_011534288.1:p.Met1093Ile
XM_011535987.1:c.2898G>A	XP_011534289.1:p.Met966Ile
XM_011535988.1:c.1761G>A	XP_011534290.1:p.Met587Ile
NM_001346813.1:c.4620G>A	NP_001333742.1:p.Met1540Ile
NM_001363725.1:c.2370G>A	NP_001350654.1:p.Met790Ile
XM_011535984.2:c.4830G>A	XP_011534286.2:p.Met1610Ile
XM_011535988.3:c.1761G>A	XP_011534290.1:p.Met587Ile
XM_017011103.2:c.4731G>A	XP_016866592.1:p.Met1577Ile
XM_017011104.1:c.4701G>A	XP_016866593.1:p.Met1567Ile
XM_017011105.2:c.4671G>A	XP_016866594.1:p.Met1557Ile
XM_017011106.2:c.4542G>A	XP_016866595.1:p.Met1514Ile
XM_017011107.2:c.4521G>A	XP_016866596.1:p.Met1507Ile
XR_002956289.1:n.4816G>A
NM_001363725.2:c.2370G>A	NP_001350654.1:p.Met790Ile
NM_001371656.1:c.4749G>A	NP_001358585.1:p.Met1583Ile
NM_001374820.1:c.4749G>A	NP_001361749.1:p.Met1583Ile
NM_001374828.1:c.4869G>A MANE Select	NP_001361757.1:p.Met1623Ile
NM_017519.3:c.4710G>A	NP_059989.3:p.Met1570Ile