Canonical Allele Identifier: CA366235293

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511245A>C (hg19) ; chr6:g.157190111A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190111A>C , CM000668.2:g.157190111A>C	GRCh38
NC_000006.11:g.157511245A>C , CM000668.1:g.157511245A>C	GRCh37
NC_000006.10:g.157552937A>C	NCBI36
NG_032093.1:g.417182A>C
NG_032093.2:g.417182A>C
NG_066624.1:g.419086A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3973A>C	ENSP00000055163.8:p.Thr1325Pro
ENST00000414678.8:c.4042A>C	ENSP00000412835.3:p.Thr1348Pro
ENST00000637015.2:c.4261A>C	ENSP00000489729.2:p.Thr1421Pro
ENST00000346085.10:c.4012A>C	ENSP00000344546.5:p.Thr1338Pro
ENST00000350026.10:c.3724A>C	ENSP00000055163.7:p.Thr1242Pro
ENST00000414678.7:c.2290A>C	ENSP00000412835.2:p.Thr764Pro
ENST00000635849.1:c.1453A>C	ENSP00000490948.1:p.Thr485Pro
ENST00000635957.1:c.1084A>C	ENSP00000490385.1:p.Thr362Pro
ENST00000636930.2:c.4132A>C MANE Select	ENSP00000490491.2:p.Thr1378Pro
ENST00000636940.1:n.2129A>C
ENST00000637015.1:c.1500A>C
ENST00000637568.1:c.1414A>C
ENST00000637741.1:n.798A>C
ENST00000637810.1:c.1474A>C	ENSP00000489636.1:p.Thr492Pro
ENST00000637904.1:c.1633A>C	ENSP00000490550.1:p.Thr545Pro
ENST00000647938.1:c.3763A>C	ENSP00000498155.1:p.Thr1255Pro
ENST00000346085.9:c.3763A>C	ENSP00000344546.4:p.Thr1255Pro
ENST00000350026.9:c.3724A>C	ENSP00000055163.7:p.Thr1242Pro
ENST00000414678.6:c.2290A>C	ENSP00000412835.2:p.Thr764Pro
NM_017519.2:c.3724A>C	NP_059989.2:p.Thr1242Pro
NM_020732.3:c.3763A>C	NP_065783.3:p.Thr1255Pro
XM_005267069.3:c.3883A>C	XP_005267126.2:p.Thr1295Pro
XM_011535984.1:c.2962A>C	XP_011534286.1:p.Thr988Pro
XM_011535985.1:c.2782A>C	XP_011534287.1:p.Thr928Pro
XM_011535986.1:c.2542A>C	XP_011534288.1:p.Thr848Pro
XM_011535987.1:c.2161A>C	XP_011534289.1:p.Thr721Pro
XM_011535988.1:c.1024A>C	XP_011534290.1:p.Thr342Pro
NM_001346813.1:c.3883A>C	NP_001333742.1:p.Thr1295Pro
NM_001363725.1:c.1633A>C	NP_001350654.1:p.Thr545Pro
XM_011535984.2:c.4093A>C	XP_011534286.2:p.Thr1365Pro
XM_011535988.3:c.1024A>C	XP_011534290.1:p.Thr342Pro
XM_017011103.2:c.3994A>C	XP_016866592.1:p.Thr1332Pro
XM_017011104.1:c.3964A>C	XP_016866593.1:p.Thr1322Pro
XM_017011105.2:c.3934A>C	XP_016866594.1:p.Thr1312Pro
XM_017011106.2:c.3805A>C	XP_016866595.1:p.Thr1269Pro
XM_017011107.2:c.3784A>C	XP_016866596.1:p.Thr1262Pro
XR_002956289.1:n.4176A>C
NM_001363725.2:c.1633A>C	NP_001350654.1:p.Thr545Pro
NM_001371656.1:c.4012A>C	NP_001358585.1:p.Thr1338Pro
NM_001374820.1:c.4012A>C	NP_001361749.1:p.Thr1338Pro
NM_001374828.1:c.4132A>C MANE Select	NP_001361757.1:p.Thr1378Pro
NM_017519.3:c.3973A>C	NP_059989.3:p.Thr1325Pro