Canonical Allele Identifier: CA366235321

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511258C>A (hg19) ; chr6:g.157190124C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190124C>A , CM000668.2:g.157190124C>A	GRCh38
NC_000006.11:g.157511258C>A , CM000668.1:g.157511258C>A	GRCh37
NC_000006.10:g.157552950C>A	NCBI36
NG_032093.1:g.417195C>A
NG_032093.2:g.417195C>A
NG_066624.1:g.419099C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3986C>A	ENSP00000055163.8:p.Pro1329His
ENST00000414678.8:c.4055C>A	ENSP00000412835.3:p.Pro1352His
ENST00000637015.2:c.4274C>A	ENSP00000489729.2:p.Pro1425His
ENST00000346085.10:c.4025C>A	ENSP00000344546.5:p.Pro1342His
ENST00000350026.10:c.3737C>A	ENSP00000055163.7:p.Pro1246His
ENST00000414678.7:c.2303C>A	ENSP00000412835.2:p.Pro768His
ENST00000635849.1:c.1466C>A	ENSP00000490948.1:p.Pro489His
ENST00000635957.1:c.1097C>A	ENSP00000490385.1:p.Pro366His
ENST00000636930.2:c.4145C>A MANE Select	ENSP00000490491.2:p.Pro1382His
ENST00000636940.1:n.2142C>A
ENST00000637015.1:c.1513C>A
ENST00000637568.1:c.1427C>A
ENST00000637741.1:n.811C>A
ENST00000637810.1:c.1487C>A	ENSP00000489636.1:p.Pro496His
ENST00000637904.1:c.1646C>A	ENSP00000490550.1:p.Pro549His
ENST00000647938.1:c.3776C>A	ENSP00000498155.1:p.Pro1259His
ENST00000346085.9:c.3776C>A	ENSP00000344546.4:p.Pro1259His
ENST00000350026.9:c.3737C>A	ENSP00000055163.7:p.Pro1246His
ENST00000414678.6:c.2303C>A	ENSP00000412835.2:p.Pro768His
NM_017519.2:c.3737C>A	NP_059989.2:p.Pro1246His
NM_020732.3:c.3776C>A	NP_065783.3:p.Pro1259His
XM_005267069.3:c.3896C>A	XP_005267126.2:p.Pro1299His
XM_011535984.1:c.2975C>A	XP_011534286.1:p.Pro992His
XM_011535985.1:c.2795C>A	XP_011534287.1:p.Pro932His
XM_011535986.1:c.2555C>A	XP_011534288.1:p.Pro852His
XM_011535987.1:c.2174C>A	XP_011534289.1:p.Pro725His
XM_011535988.1:c.1037C>A	XP_011534290.1:p.Pro346His
NM_001346813.1:c.3896C>A	NP_001333742.1:p.Pro1299His
NM_001363725.1:c.1646C>A	NP_001350654.1:p.Pro549His
XM_011535984.2:c.4106C>A	XP_011534286.2:p.Pro1369His
XM_011535988.3:c.1037C>A	XP_011534290.1:p.Pro346His
XM_017011103.2:c.4007C>A	XP_016866592.1:p.Pro1336His
XM_017011104.1:c.3977C>A	XP_016866593.1:p.Pro1326His
XM_017011105.2:c.3947C>A	XP_016866594.1:p.Pro1316His
XM_017011106.2:c.3818C>A	XP_016866595.1:p.Pro1273His
XM_017011107.2:c.3797C>A	XP_016866596.1:p.Pro1266His
XR_002956289.1:n.4189C>A
NM_001363725.2:c.1646C>A	NP_001350654.1:p.Pro549His
NM_001371656.1:c.4025C>A	NP_001358585.1:p.Pro1342His
NM_001374820.1:c.4025C>A	NP_001361749.1:p.Pro1342His
NM_001374828.1:c.4145C>A MANE Select	NP_001361757.1:p.Pro1382His
NM_017519.3:c.3986C>A	NP_059989.3:p.Pro1329His