Canonical Allele Identifier: CA366242149

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522297G>T (hg19) ; chr6:g.157201163G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201163G>T , CM000668.2:g.157201163G>T	GRCh38
NC_000006.11:g.157522297G>T , CM000668.1:g.157522297G>T	GRCh37
NC_000006.10:g.157563989G>T	NCBI36
NG_032093.1:g.428234G>T
NG_032093.2:g.428234G>T
NG_066624.1:g.430138G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4779G>T	ENSP00000055163.8:p.Met1593Ile
ENST00000414678.8:c.4848G>T	ENSP00000412835.3:p.Met1616Ile
ENST00000637015.2:c.5067G>T	ENSP00000489729.2:p.Met1689Ile
ENST00000346085.10:c.4818G>T	ENSP00000344546.5:p.Met1606Ile
ENST00000350026.10:c.4530G>T	ENSP00000055163.7:p.Met1510Ile
ENST00000414678.7:c.3096G>T	ENSP00000412835.2:p.Met1032Ile
ENST00000635849.1:c.2259G>T	ENSP00000490948.1:p.Met753Ile
ENST00000635957.1:c.1890G>T	ENSP00000490385.1:p.Met630Ile
ENST00000636227.1:n.3401G>T
ENST00000636254.1:n.858G>T
ENST00000636930.2:c.4938G>T MANE Select	ENSP00000490491.2:p.Met1646Ile
ENST00000636940.1:n.2935G>T
ENST00000637015.1:c.2306G>T
ENST00000637568.1:c.2220G>T
ENST00000637741.1:n.1604G>T
ENST00000637810.1:c.2280G>T	ENSP00000489636.1:p.Met760Ile
ENST00000637904.1:c.2439G>T	ENSP00000490550.1:p.Met813Ile
ENST00000647938.1:c.4569G>T	ENSP00000498155.1:p.Met1523Ile
ENST00000346085.9:c.4569G>T	ENSP00000344546.4:p.Met1523Ile
ENST00000350026.9:c.4530G>T	ENSP00000055163.7:p.Met1510Ile
ENST00000414678.6:c.3096G>T	ENSP00000412835.2:p.Met1032Ile
NM_017519.2:c.4530G>T	NP_059989.2:p.Met1510Ile
NM_020732.3:c.4569G>T	NP_065783.3:p.Met1523Ile
XM_005267069.3:c.4689G>T	XP_005267126.2:p.Met1563Ile
XM_011535984.1:c.3768G>T	XP_011534286.1:p.Met1256Ile
XM_011535985.1:c.3588G>T	XP_011534287.1:p.Met1196Ile
XM_011535986.1:c.3348G>T	XP_011534288.1:p.Met1116Ile
XM_011535987.1:c.2967G>T	XP_011534289.1:p.Met989Ile
XM_011535988.1:c.1830G>T	XP_011534290.1:p.Met610Ile
NM_001346813.1:c.4689G>T	NP_001333742.1:p.Met1563Ile
NM_001363725.1:c.2439G>T	NP_001350654.1:p.Met813Ile
XM_011535984.2:c.4899G>T	XP_011534286.2:p.Met1633Ile
XM_011535988.3:c.1830G>T	XP_011534290.1:p.Met610Ile
XM_017011103.2:c.4800G>T	XP_016866592.1:p.Met1600Ile
XM_017011104.1:c.4770G>T	XP_016866593.1:p.Met1590Ile
XM_017011105.2:c.4740G>T	XP_016866594.1:p.Met1580Ile
XM_017011106.2:c.4611G>T	XP_016866595.1:p.Met1537Ile
XM_017011107.2:c.4590G>T	XP_016866596.1:p.Met1530Ile
XR_002956289.1:n.4885G>T
NM_001363725.2:c.2439G>T	NP_001350654.1:p.Met813Ile
NM_001371656.1:c.4818G>T	NP_001358585.1:p.Met1606Ile
NM_001374820.1:c.4818G>T	NP_001361749.1:p.Met1606Ile
NM_001374828.1:c.4938G>T MANE Select	NP_001361757.1:p.Met1646Ile
NM_017519.3:c.4779G>T	NP_059989.3:p.Met1593Ile