Canonical Allele Identifier: CA366234087

Gene: ARID1B

Linked Data

• COSMIC: COSM6173061 ; COSM6173062
• MyVariant Identifiers: chr6:g.157510821G>C (hg19) ; chr6:g.157189687G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189687G>C , CM000668.2:g.157189687G>C	GRCh38
NC_000006.11:g.157510821G>C , CM000668.1:g.157510821G>C	GRCh37
NC_000006.10:g.157552513G>C	NCBI36
NG_032093.1:g.416758G>C
NG_032093.2:g.416758G>C
NG_066624.1:g.418662G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3806G>C	ENSP00000055163.8:p.Gly1269Ala
ENST00000414678.8:c.3875G>C	ENSP00000412835.3:p.Gly1292Ala
ENST00000637015.2:c.4094G>C	ENSP00000489729.2:p.Gly1365Ala
ENST00000346085.10:c.3845G>C	ENSP00000344546.5:p.Gly1282Ala
ENST00000350026.10:c.3557G>C	ENSP00000055163.7:p.Gly1186Ala
ENST00000414678.7:c.2123G>C	ENSP00000412835.2:p.Gly708Ala
ENST00000635849.1:c.1286G>C	ENSP00000490948.1:p.Gly429Ala
ENST00000635957.1:c.920G>C	ENSP00000490385.1:p.Gly307Ala
ENST00000636930.2:c.3965G>C MANE Select	ENSP00000490491.2:p.Gly1322Ala
ENST00000636940.1:n.1962G>C
ENST00000637015.1:c.1333G>C
ENST00000637568.1:c.1247G>C
ENST00000637741.1:n.631G>C
ENST00000637810.1:c.1307G>C	ENSP00000489636.1:p.Gly436Ala
ENST00000637904.1:c.1466G>C	ENSP00000490550.1:p.Gly489Ala
ENST00000647938.1:c.3596G>C	ENSP00000498155.1:p.Gly1199Ala
ENST00000346085.9:c.3596G>C	ENSP00000344546.4:p.Gly1199Ala
ENST00000350026.9:c.3557G>C	ENSP00000055163.7:p.Gly1186Ala
ENST00000414678.6:c.2123G>C	ENSP00000412835.2:p.Gly708Ala
NM_017519.2:c.3557G>C	NP_059989.2:p.Gly1186Ala
NM_020732.3:c.3596G>C	NP_065783.3:p.Gly1199Ala
XM_005267069.3:c.3716G>C	XP_005267126.2:p.Gly1239Ala
XM_011535984.1:c.2795G>C	XP_011534286.1:p.Gly932Ala
XM_011535985.1:c.2615G>C	XP_011534287.1:p.Gly872Ala
XM_011535986.1:c.2375G>C	XP_011534288.1:p.Gly792Ala
XM_011535987.1:c.1994G>C	XP_011534289.1:p.Gly665Ala
XM_011535988.1:c.857G>C	XP_011534290.1:p.Gly286Ala
NM_001346813.1:c.3716G>C	NP_001333742.1:p.Gly1239Ala
NM_001363725.1:c.1466G>C	NP_001350654.1:p.Gly489Ala
XM_011535984.2:c.3926G>C	XP_011534286.2:p.Gly1309Ala
XM_011535988.3:c.857G>C	XP_011534290.1:p.Gly286Ala
XM_017011103.2:c.3827G>C	XP_016866592.1:p.Gly1276Ala
XM_017011104.1:c.3797G>C	XP_016866593.1:p.Gly1266Ala
XM_017011105.2:c.3767G>C	XP_016866594.1:p.Gly1256Ala
XM_017011106.2:c.3638G>C	XP_016866595.1:p.Gly1213Ala
XM_017011107.2:c.3617G>C	XP_016866596.1:p.Gly1206Ala
XR_002956289.1:n.4009G>C
NM_001363725.2:c.1466G>C	NP_001350654.1:p.Gly489Ala
NM_001371656.1:c.3845G>C	NP_001358585.1:p.Gly1282Ala
NM_001374820.1:c.3845G>C	NP_001361749.1:p.Gly1282Ala
NM_001374828.1:c.3965G>C MANE Select	NP_001361757.1:p.Gly1322Ala
NM_017519.3:c.3806G>C	NP_059989.3:p.Gly1269Ala