Canonical Allele Identifier: CA452781505

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510801A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189667A>T , CM000668.2:g.157189667A>T	GRCh38
NC_000006.11:g.157510801A>T , CM000668.1:g.157510801A>T	GRCh37
NC_000006.10:g.157552493A>T	NCBI36
NG_032093.1:g.416738A>T
NG_032093.2:g.416738A>T
NG_066624.1:g.418642A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3786A>T	ENSP00000055163.8:p.Pro1262=
ENST00000414678.8:c.3855A>T	ENSP00000412835.3:p.Pro1285=
ENST00000637015.2:c.4074A>T	ENSP00000489729.2:p.Pro1358=
ENST00000346085.10:c.3825A>T	ENSP00000344546.5:p.Pro1275=
ENST00000350026.10:c.3537A>T	ENSP00000055163.7:p.Pro1179=
ENST00000414678.7:c.2103A>T	ENSP00000412835.2:p.Pro701=
ENST00000635849.1:c.1266A>T	ENSP00000490948.1:p.Pro422=
ENST00000635957.1:c.900A>T	ENSP00000490385.1:p.Pro300=
ENST00000636930.2:c.3945A>T MANE Select	ENSP00000490491.2:p.Pro1315=
ENST00000636940.1:n.1942A>T
ENST00000637015.1:c.1313A>T
ENST00000637568.1:c.1227A>T
ENST00000637741.1:n.611A>T
ENST00000637810.1:c.1287A>T	ENSP00000489636.1:p.Pro429=
ENST00000637904.1:c.1446A>T	ENSP00000490550.1:p.Pro482=
ENST00000647938.1:c.3576A>T	ENSP00000498155.1:p.Pro1192=
ENST00000346085.9:c.3576A>T	ENSP00000344546.4:p.Pro1192=
ENST00000350026.9:c.3537A>T	ENSP00000055163.7:p.Pro1179=
ENST00000414678.6:c.2103A>T	ENSP00000412835.2:p.Pro701=
NM_017519.2:c.3537A>T	NP_059989.2:p.Pro1179=
NM_020732.3:c.3576A>T	NP_065783.3:p.Pro1192=
XM_005267069.3:c.3696A>T	XP_005267126.2:p.Pro1232=
XM_011535984.1:c.2775A>T	XP_011534286.1:p.Pro925=
XM_011535985.1:c.2595A>T	XP_011534287.1:p.Pro865=
XM_011535986.1:c.2355A>T	XP_011534288.1:p.Pro785=
XM_011535987.1:c.1974A>T	XP_011534289.1:p.Pro658=
XM_011535988.1:c.837A>T	XP_011534290.1:p.Pro279=
NM_001346813.1:c.3696A>T	NP_001333742.1:p.Pro1232=
NM_001363725.1:c.1446A>T	NP_001350654.1:p.Pro482=
XM_011535984.2:c.3906A>T	XP_011534286.2:p.Pro1302=
XM_011535988.3:c.837A>T	XP_011534290.1:p.Pro279=
XM_017011103.2:c.3807A>T	XP_016866592.1:p.Pro1269=
XM_017011104.1:c.3777A>T	XP_016866593.1:p.Pro1259=
XM_017011105.2:c.3747A>T	XP_016866594.1:p.Pro1249=
XM_017011106.2:c.3618A>T	XP_016866595.1:p.Pro1206=
XM_017011107.2:c.3597A>T	XP_016866596.1:p.Pro1199=
XR_002956289.1:n.3989A>T
NM_001363725.2:c.1446A>T	NP_001350654.1:p.Pro482=
NM_001371656.1:c.3825A>T	NP_001358585.1:p.Pro1275=
NM_001374820.1:c.3825A>T	NP_001361749.1:p.Pro1275=
NM_001374828.1:c.3945A>T MANE Select	NP_001361757.1:p.Pro1315=
NM_017519.3:c.3786A>T	NP_059989.3:p.Pro1262=