Canonical Allele Identifier: CA366241368

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522118A>G (hg19) ; chr6:g.157200984A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200984A>G , CM000668.2:g.157200984A>G	GRCh38
NC_000006.11:g.157522118A>G , CM000668.1:g.157522118A>G	GRCh37
NC_000006.10:g.157563810A>G	NCBI36
NG_032093.1:g.428055A>G
NG_032093.2:g.428055A>G
NG_066624.1:g.429959A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4600A>G	ENSP00000055163.8:p.Met1534Val
ENST00000414678.8:c.4669A>G	ENSP00000412835.3:p.Met1557Val
ENST00000637015.2:c.4888A>G	ENSP00000489729.2:p.Met1630Val
ENST00000346085.10:c.4639A>G	ENSP00000344546.5:p.Met1547Val
ENST00000350026.10:c.4351A>G	ENSP00000055163.7:p.Met1451Val
ENST00000414678.7:c.2917A>G	ENSP00000412835.2:p.Met973Val
ENST00000635849.1:c.2080A>G	ENSP00000490948.1:p.Met694Val
ENST00000635957.1:c.1711A>G	ENSP00000490385.1:p.Met571Val
ENST00000636227.1:n.3222A>G
ENST00000636254.1:n.679A>G
ENST00000636930.2:c.4759A>G MANE Select	ENSP00000490491.2:p.Met1587Val
ENST00000636940.1:n.2756A>G
ENST00000637015.1:c.2127A>G
ENST00000637568.1:c.2041A>G
ENST00000637741.1:n.1425A>G
ENST00000637810.1:c.2101A>G	ENSP00000489636.1:p.Met701Val
ENST00000637904.1:c.2260A>G	ENSP00000490550.1:p.Met754Val
ENST00000647938.1:c.4390A>G	ENSP00000498155.1:p.Met1464Val
ENST00000346085.9:c.4390A>G	ENSP00000344546.4:p.Met1464Val
ENST00000350026.9:c.4351A>G	ENSP00000055163.7:p.Met1451Val
ENST00000414678.6:c.2917A>G	ENSP00000412835.2:p.Met973Val
NM_017519.2:c.4351A>G	NP_059989.2:p.Met1451Val
NM_020732.3:c.4390A>G	NP_065783.3:p.Met1464Val
XM_005267069.3:c.4510A>G	XP_005267126.2:p.Met1504Val
XM_011535984.1:c.3589A>G	XP_011534286.1:p.Met1197Val
XM_011535985.1:c.3409A>G	XP_011534287.1:p.Met1137Val
XM_011535986.1:c.3169A>G	XP_011534288.1:p.Met1057Val
XM_011535987.1:c.2788A>G	XP_011534289.1:p.Met930Val
XM_011535988.1:c.1651A>G	XP_011534290.1:p.Met551Val
NM_001346813.1:c.4510A>G	NP_001333742.1:p.Met1504Val
NM_001363725.1:c.2260A>G	NP_001350654.1:p.Met754Val
XM_011535984.2:c.4720A>G	XP_011534286.2:p.Met1574Val
XM_011535988.3:c.1651A>G	XP_011534290.1:p.Met551Val
XM_017011103.2:c.4621A>G	XP_016866592.1:p.Met1541Val
XM_017011104.1:c.4591A>G	XP_016866593.1:p.Met1531Val
XM_017011105.2:c.4561A>G	XP_016866594.1:p.Met1521Val
XM_017011106.2:c.4432A>G	XP_016866595.1:p.Met1478Val
XM_017011107.2:c.4411A>G	XP_016866596.1:p.Met1471Val
XR_002956289.1:n.4706A>G
NM_001363725.2:c.2260A>G	NP_001350654.1:p.Met754Val
NM_001371656.1:c.4639A>G	NP_001358585.1:p.Met1547Val
NM_001374820.1:c.4639A>G	NP_001361749.1:p.Met1547Val
NM_001374828.1:c.4759A>G MANE Select	NP_001361757.1:p.Met1587Val
NM_017519.3:c.4600A>G	NP_059989.3:p.Met1534Val