Canonical Allele Identifier: CA366241469

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522141G>T (hg19) ; chr6:g.157201007G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201007G>T , CM000668.2:g.157201007G>T	GRCh38
NC_000006.11:g.157522141G>T , CM000668.1:g.157522141G>T	GRCh37
NC_000006.10:g.157563833G>T	NCBI36
NG_032093.1:g.428078G>T
NG_032093.2:g.428078G>T
NG_066624.1:g.429982G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4623G>T	ENSP00000055163.8:p.Met1541Ile
ENST00000414678.8:c.4692G>T	ENSP00000412835.3:p.Met1564Ile
ENST00000637015.2:c.4911G>T	ENSP00000489729.2:p.Met1637Ile
ENST00000346085.10:c.4662G>T	ENSP00000344546.5:p.Met1554Ile
ENST00000350026.10:c.4374G>T	ENSP00000055163.7:p.Met1458Ile
ENST00000414678.7:c.2940G>T	ENSP00000412835.2:p.Met980Ile
ENST00000635849.1:c.2103G>T	ENSP00000490948.1:p.Met701Ile
ENST00000635957.1:c.1734G>T	ENSP00000490385.1:p.Met578Ile
ENST00000636227.1:n.3245G>T
ENST00000636254.1:n.702G>T
ENST00000636930.2:c.4782G>T MANE Select	ENSP00000490491.2:p.Met1594Ile
ENST00000636940.1:n.2779G>T
ENST00000637015.1:c.2150G>T
ENST00000637568.1:c.2064G>T
ENST00000637741.1:n.1448G>T
ENST00000637810.1:c.2124G>T	ENSP00000489636.1:p.Met708Ile
ENST00000637904.1:c.2283G>T	ENSP00000490550.1:p.Met761Ile
ENST00000647938.1:c.4413G>T	ENSP00000498155.1:p.Met1471Ile
ENST00000346085.9:c.4413G>T	ENSP00000344546.4:p.Met1471Ile
ENST00000350026.9:c.4374G>T	ENSP00000055163.7:p.Met1458Ile
ENST00000414678.6:c.2940G>T	ENSP00000412835.2:p.Met980Ile
NM_017519.2:c.4374G>T	NP_059989.2:p.Met1458Ile
NM_020732.3:c.4413G>T	NP_065783.3:p.Met1471Ile
XM_005267069.3:c.4533G>T	XP_005267126.2:p.Met1511Ile
XM_011535984.1:c.3612G>T	XP_011534286.1:p.Met1204Ile
XM_011535985.1:c.3432G>T	XP_011534287.1:p.Met1144Ile
XM_011535986.1:c.3192G>T	XP_011534288.1:p.Met1064Ile
XM_011535987.1:c.2811G>T	XP_011534289.1:p.Met937Ile
XM_011535988.1:c.1674G>T	XP_011534290.1:p.Met558Ile
NM_001346813.1:c.4533G>T	NP_001333742.1:p.Met1511Ile
NM_001363725.1:c.2283G>T	NP_001350654.1:p.Met761Ile
XM_011535984.2:c.4743G>T	XP_011534286.2:p.Met1581Ile
XM_011535988.3:c.1674G>T	XP_011534290.1:p.Met558Ile
XM_017011103.2:c.4644G>T	XP_016866592.1:p.Met1548Ile
XM_017011104.1:c.4614G>T	XP_016866593.1:p.Met1538Ile
XM_017011105.2:c.4584G>T	XP_016866594.1:p.Met1528Ile
XM_017011106.2:c.4455G>T	XP_016866595.1:p.Met1485Ile
XM_017011107.2:c.4434G>T	XP_016866596.1:p.Met1478Ile
XR_002956289.1:n.4729G>T
NM_001363725.2:c.2283G>T	NP_001350654.1:p.Met761Ile
NM_001371656.1:c.4662G>T	NP_001358585.1:p.Met1554Ile
NM_001374820.1:c.4662G>T	NP_001361749.1:p.Met1554Ile
NM_001374828.1:c.4782G>T MANE Select	NP_001361757.1:p.Met1594Ile
NM_017519.3:c.4623G>T	NP_059989.3:p.Met1541Ile