Canonical Allele Identifier: CA452781531

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510846A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189712A>C , CM000668.2:g.157189712A>C	GRCh38
NC_000006.11:g.157510846A>C , CM000668.1:g.157510846A>C	GRCh37
NC_000006.10:g.157552538A>C	NCBI36
NG_032093.1:g.416783A>C
NG_032093.2:g.416783A>C
NG_066624.1:g.418687A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3831A>C	ENSP00000055163.8:p.Pro1277=
ENST00000414678.8:c.3900A>C	ENSP00000412835.3:p.Pro1300=
ENST00000637015.2:c.4119A>C	ENSP00000489729.2:p.Pro1373=
ENST00000346085.10:c.3870A>C	ENSP00000344546.5:p.Pro1290=
ENST00000350026.10:c.3582A>C	ENSP00000055163.7:p.Pro1194=
ENST00000414678.7:c.2148A>C	ENSP00000412835.2:p.Pro716=
ENST00000635849.1:c.1311A>C	ENSP00000490948.1:p.Pro437=
ENST00000635957.1:c.945A>C	ENSP00000490385.1:p.Pro315=
ENST00000636930.2:c.3990A>C MANE Select	ENSP00000490491.2:p.Pro1330=
ENST00000636940.1:n.1987A>C
ENST00000637015.1:c.1358A>C
ENST00000637568.1:c.1272A>C
ENST00000637741.1:n.656A>C
ENST00000637810.1:c.1332A>C	ENSP00000489636.1:p.Pro444=
ENST00000637904.1:c.1491A>C	ENSP00000490550.1:p.Pro497=
ENST00000647938.1:c.3621A>C	ENSP00000498155.1:p.Pro1207=
ENST00000346085.9:c.3621A>C	ENSP00000344546.4:p.Pro1207=
ENST00000350026.9:c.3582A>C	ENSP00000055163.7:p.Pro1194=
ENST00000414678.6:c.2148A>C	ENSP00000412835.2:p.Pro716=
NM_017519.2:c.3582A>C	NP_059989.2:p.Pro1194=
NM_020732.3:c.3621A>C	NP_065783.3:p.Pro1207=
XM_005267069.3:c.3741A>C	XP_005267126.2:p.Pro1247=
XM_011535984.1:c.2820A>C	XP_011534286.1:p.Pro940=
XM_011535985.1:c.2640A>C	XP_011534287.1:p.Pro880=
XM_011535986.1:c.2400A>C	XP_011534288.1:p.Pro800=
XM_011535987.1:c.2019A>C	XP_011534289.1:p.Pro673=
XM_011535988.1:c.882A>C	XP_011534290.1:p.Pro294=
NM_001346813.1:c.3741A>C	NP_001333742.1:p.Pro1247=
NM_001363725.1:c.1491A>C	NP_001350654.1:p.Pro497=
XM_011535984.2:c.3951A>C	XP_011534286.2:p.Pro1317=
XM_011535988.3:c.882A>C	XP_011534290.1:p.Pro294=
XM_017011103.2:c.3852A>C	XP_016866592.1:p.Pro1284=
XM_017011104.1:c.3822A>C	XP_016866593.1:p.Pro1274=
XM_017011105.2:c.3792A>C	XP_016866594.1:p.Pro1264=
XM_017011106.2:c.3663A>C	XP_016866595.1:p.Pro1221=
XM_017011107.2:c.3642A>C	XP_016866596.1:p.Pro1214=
XR_002956289.1:n.4034A>C
NM_001363725.2:c.1491A>C	NP_001350654.1:p.Pro497=
NM_001371656.1:c.3870A>C	NP_001358585.1:p.Pro1290=
NM_001374820.1:c.3870A>C	NP_001361749.1:p.Pro1290=
NM_001374828.1:c.3990A>C MANE Select	NP_001361757.1:p.Pro1330=
NM_017519.3:c.3831A>C	NP_059989.3:p.Pro1277=