Canonical Allele Identifier: CA366241542

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522155A>C (hg19) ; chr6:g.157201021A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201021A>C , CM000668.2:g.157201021A>C	GRCh38
NC_000006.11:g.157522155A>C , CM000668.1:g.157522155A>C	GRCh37
NC_000006.10:g.157563847A>C	NCBI36
NG_032093.1:g.428092A>C
NG_032093.2:g.428092A>C
NG_066624.1:g.429996A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4637A>C	ENSP00000055163.8:p.Gln1546Pro
ENST00000414678.8:c.4706A>C	ENSP00000412835.3:p.Gln1569Pro
ENST00000637015.2:c.4925A>C	ENSP00000489729.2:p.Gln1642Pro
ENST00000346085.10:c.4676A>C	ENSP00000344546.5:p.Gln1559Pro
ENST00000350026.10:c.4388A>C	ENSP00000055163.7:p.Gln1463Pro
ENST00000414678.7:c.2954A>C	ENSP00000412835.2:p.Gln985Pro
ENST00000635849.1:c.2117A>C	ENSP00000490948.1:p.Gln706Pro
ENST00000635957.1:c.1748A>C	ENSP00000490385.1:p.Gln583Pro
ENST00000636227.1:n.3259A>C
ENST00000636254.1:n.716A>C
ENST00000636930.2:c.4796A>C MANE Select	ENSP00000490491.2:p.Gln1599Pro
ENST00000636940.1:n.2793A>C
ENST00000637015.1:c.2164A>C
ENST00000637568.1:c.2078A>C
ENST00000637741.1:n.1462A>C
ENST00000637810.1:c.2138A>C	ENSP00000489636.1:p.Gln713Pro
ENST00000637904.1:c.2297A>C	ENSP00000490550.1:p.Gln766Pro
ENST00000647938.1:c.4427A>C	ENSP00000498155.1:p.Gln1476Pro
ENST00000346085.9:c.4427A>C	ENSP00000344546.4:p.Gln1476Pro
ENST00000350026.9:c.4388A>C	ENSP00000055163.7:p.Gln1463Pro
ENST00000414678.6:c.2954A>C	ENSP00000412835.2:p.Gln985Pro
NM_017519.2:c.4388A>C	NP_059989.2:p.Gln1463Pro
NM_020732.3:c.4427A>C	NP_065783.3:p.Gln1476Pro
XM_005267069.3:c.4547A>C	XP_005267126.2:p.Gln1516Pro
XM_011535984.1:c.3626A>C	XP_011534286.1:p.Gln1209Pro
XM_011535985.1:c.3446A>C	XP_011534287.1:p.Gln1149Pro
XM_011535986.1:c.3206A>C	XP_011534288.1:p.Gln1069Pro
XM_011535987.1:c.2825A>C	XP_011534289.1:p.Gln942Pro
XM_011535988.1:c.1688A>C	XP_011534290.1:p.Gln563Pro
NM_001346813.1:c.4547A>C	NP_001333742.1:p.Gln1516Pro
NM_001363725.1:c.2297A>C	NP_001350654.1:p.Gln766Pro
XM_011535984.2:c.4757A>C	XP_011534286.2:p.Gln1586Pro
XM_011535988.3:c.1688A>C	XP_011534290.1:p.Gln563Pro
XM_017011103.2:c.4658A>C	XP_016866592.1:p.Gln1553Pro
XM_017011104.1:c.4628A>C	XP_016866593.1:p.Gln1543Pro
XM_017011105.2:c.4598A>C	XP_016866594.1:p.Gln1533Pro
XM_017011106.2:c.4469A>C	XP_016866595.1:p.Gln1490Pro
XM_017011107.2:c.4448A>C	XP_016866596.1:p.Gln1483Pro
XR_002956289.1:n.4743A>C
NM_001363725.2:c.2297A>C	NP_001350654.1:p.Gln766Pro
NM_001371656.1:c.4676A>C	NP_001358585.1:p.Gln1559Pro
NM_001374820.1:c.4676A>C	NP_001361749.1:p.Gln1559Pro
NM_001374828.1:c.4796A>C MANE Select	NP_001361757.1:p.Gln1599Pro
NM_017519.3:c.4637A>C	NP_059989.3:p.Gln1546Pro