Canonical Allele Identifier: CA150359257

Gene: ARID1B

Linked Data

• dbSNP Id: rs746686035
• MyVariant Identifiers: chr6:g.157502256C>T (hg19) ; chr6:g.157181122C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181122C>T , CM000668.2:g.157181122C>T	GRCh38
NC_000006.11:g.157502256C>T , CM000668.1:g.157502256C>T	GRCh37
NC_000006.10:g.157543948C>T	NCBI36
NG_032093.1:g.408193C>T
NG_032093.2:g.408193C>T
NG_066624.1:g.410097C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3499C>T	ENSP00000055163.8:p.Pro1167Ser
ENST00000414678.8:c.3568C>T	ENSP00000412835.3:p.Pro1190Ser
ENST00000637015.2:c.3787C>T	ENSP00000489729.2:p.Pro1263Ser
ENST00000319584.11:c.1672C>T	ENSP00000313006.7:p.Pro558Ser
ENST00000346085.10:c.3538C>T	ENSP00000344546.5:p.Pro1180Ser
ENST00000350026.10:c.3250C>T	ENSP00000055163.7:p.Pro1084Ser
ENST00000414678.7:c.1816C>T	ENSP00000412835.2:p.Pro606Ser
ENST00000635849.1:c.979C>T	ENSP00000490948.1:p.Pro327Ser
ENST00000635957.1:c.613C>T	ENSP00000490385.1:p.Pro205Ser
ENST00000636930.2:c.3658C>T MANE Select	ENSP00000490491.2:p.Pro1220Ser
ENST00000636940.1:n.1655C>T
ENST00000637015.1:c.1026C>T
ENST00000637568.1:c.940C>T
ENST00000637741.1:n.324C>T
ENST00000637810.1:c.1000C>T	ENSP00000489636.1:p.Pro334Ser
ENST00000637904.1:c.1159C>T	ENSP00000490550.1:p.Pro387Ser
ENST00000647938.1:c.3289C>T	ENSP00000498155.1:p.Pro1097Ser
ENST00000319584.10:c.1675C>T	ENSP00000313006.6:p.Pro559Ser
ENST00000346085.9:c.3289C>T	ENSP00000344546.4:p.Pro1097Ser
ENST00000350026.9:c.3250C>T	ENSP00000055163.7:p.Pro1084Ser
ENST00000400790.3:c.451C>T	ENSP00000383596.3:p.Pro151Ser
ENST00000414678.6:c.1816C>T	ENSP00000412835.2:p.Pro606Ser
ENST00000478761.3:c.860C>T
NM_017519.2:c.3250C>T	NP_059989.2:p.Pro1084Ser
NM_020732.3:c.3289C>T	NP_065783.3:p.Pro1097Ser
XM_005267069.3:c.3409C>T	XP_005267126.2:p.Pro1137Ser
XM_011535984.1:c.2488C>T	XP_011534286.1:p.Pro830Ser
XM_011535985.1:c.2308C>T	XP_011534287.1:p.Pro770Ser
XM_011535986.1:c.2068C>T	XP_011534288.1:p.Pro690Ser
XM_011535987.1:c.1687C>T	XP_011534289.1:p.Pro563Ser
XM_011535988.1:c.550C>T	XP_011534290.1:p.Pro184Ser
NM_001346813.1:c.3409C>T	NP_001333742.1:p.Pro1137Ser
NM_001363725.1:c.1159C>T	NP_001350654.1:p.Pro387Ser
XM_011535984.2:c.3619C>T	XP_011534286.2:p.Pro1207Ser
XM_011535988.3:c.550C>T	XP_011534290.1:p.Pro184Ser
XM_017011103.2:c.3520C>T	XP_016866592.1:p.Pro1174Ser
XM_017011104.1:c.3490C>T	XP_016866593.1:p.Pro1164Ser
XM_017011105.2:c.3460C>T	XP_016866594.1:p.Pro1154Ser
XM_017011106.2:c.3331C>T	XP_016866595.1:p.Pro1111Ser
XM_017011107.2:c.3310C>T	XP_016866596.1:p.Pro1104Ser
XR_002956289.1:n.3702C>T
NM_001363725.2:c.1159C>T	NP_001350654.1:p.Pro387Ser
NM_001371656.1:c.3538C>T	NP_001358585.1:p.Pro1180Ser
NM_001374820.1:c.3538C>T	NP_001361749.1:p.Pro1180Ser
NM_001374828.1:c.3658C>T MANE Select	NP_001361757.1:p.Pro1220Ser
NM_017519.3:c.3499C>T	NP_059989.3:p.Pro1167Ser