Canonical Allele Identifier: CA366234110

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510832A>G (hg19) ; chr6:g.157189698A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189698A>G , CM000668.2:g.157189698A>G	GRCh38
NC_000006.11:g.157510832A>G , CM000668.1:g.157510832A>G	GRCh37
NC_000006.10:g.157552524A>G	NCBI36
NG_032093.1:g.416769A>G
NG_032093.2:g.416769A>G
NG_066624.1:g.418673A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3817A>G	ENSP00000055163.8:p.Met1273Val
ENST00000414678.8:c.3886A>G	ENSP00000412835.3:p.Met1296Val
ENST00000637015.2:c.4105A>G	ENSP00000489729.2:p.Met1369Val
ENST00000346085.10:c.3856A>G	ENSP00000344546.5:p.Met1286Val
ENST00000350026.10:c.3568A>G	ENSP00000055163.7:p.Met1190Val
ENST00000414678.7:c.2134A>G	ENSP00000412835.2:p.Met712Val
ENST00000635849.1:c.1297A>G	ENSP00000490948.1:p.Met433Val
ENST00000635957.1:c.931A>G	ENSP00000490385.1:p.Met311Val
ENST00000636930.2:c.3976A>G MANE Select	ENSP00000490491.2:p.Met1326Val
ENST00000636940.1:n.1973A>G
ENST00000637015.1:c.1344A>G
ENST00000637568.1:c.1258A>G
ENST00000637741.1:n.642A>G
ENST00000637810.1:c.1318A>G	ENSP00000489636.1:p.Met440Val
ENST00000637904.1:c.1477A>G	ENSP00000490550.1:p.Met493Val
ENST00000647938.1:c.3607A>G	ENSP00000498155.1:p.Met1203Val
ENST00000346085.9:c.3607A>G	ENSP00000344546.4:p.Met1203Val
ENST00000350026.9:c.3568A>G	ENSP00000055163.7:p.Met1190Val
ENST00000414678.6:c.2134A>G	ENSP00000412835.2:p.Met712Val
NM_017519.2:c.3568A>G	NP_059989.2:p.Met1190Val
NM_020732.3:c.3607A>G	NP_065783.3:p.Met1203Val
XM_005267069.3:c.3727A>G	XP_005267126.2:p.Met1243Val
XM_011535984.1:c.2806A>G	XP_011534286.1:p.Met936Val
XM_011535985.1:c.2626A>G	XP_011534287.1:p.Met876Val
XM_011535986.1:c.2386A>G	XP_011534288.1:p.Met796Val
XM_011535987.1:c.2005A>G	XP_011534289.1:p.Met669Val
XM_011535988.1:c.868A>G	XP_011534290.1:p.Met290Val
NM_001346813.1:c.3727A>G	NP_001333742.1:p.Met1243Val
NM_001363725.1:c.1477A>G	NP_001350654.1:p.Met493Val
XM_011535984.2:c.3937A>G	XP_011534286.2:p.Met1313Val
XM_011535988.3:c.868A>G	XP_011534290.1:p.Met290Val
XM_017011103.2:c.3838A>G	XP_016866592.1:p.Met1280Val
XM_017011104.1:c.3808A>G	XP_016866593.1:p.Met1270Val
XM_017011105.2:c.3778A>G	XP_016866594.1:p.Met1260Val
XM_017011106.2:c.3649A>G	XP_016866595.1:p.Met1217Val
XM_017011107.2:c.3628A>G	XP_016866596.1:p.Met1210Val
XR_002956289.1:n.4020A>G
NM_001363725.2:c.1477A>G	NP_001350654.1:p.Met493Val
NM_001371656.1:c.3856A>G	NP_001358585.1:p.Met1286Val
NM_001374820.1:c.3856A>G	NP_001361749.1:p.Met1286Val
NM_001374828.1:c.3976A>G MANE Select	NP_001361757.1:p.Met1326Val
NM_017519.3:c.3817A>G	NP_059989.3:p.Met1273Val