Canonical Allele Identifier: CA366239764

Gene: ARID1B

Linked Data

• dbSNP Id: rs577211667
• MyVariant Identifiers: chr6:g.157519998C>G (hg19) ; chr6:g.157198864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198864C>G , CM000668.2:g.157198864C>G	GRCh38
NC_000006.11:g.157519998C>G , CM000668.1:g.157519998C>G	GRCh37
NC_000006.10:g.157561690C>G	NCBI36
NG_032093.1:g.425935C>G
NG_032093.2:g.425935C>G
NG_066624.1:g.427839C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4277C>G	ENSP00000055163.8:p.Pro1426Arg
ENST00000414678.8:c.4346C>G	ENSP00000412835.3:p.Pro1449Arg
ENST00000637015.2:c.4565C>G	ENSP00000489729.2:p.Pro1522Arg
ENST00000346085.10:c.4316C>G	ENSP00000344546.5:p.Pro1439Arg
ENST00000350026.10:c.4028C>G	ENSP00000055163.7:p.Pro1343Arg
ENST00000414678.7:c.2594C>G	ENSP00000412835.2:p.Pro865Arg
ENST00000635849.1:c.1757C>G	ENSP00000490948.1:p.Pro586Arg
ENST00000635957.1:c.1388C>G	ENSP00000490385.1:p.Pro463Arg
ENST00000636227.1:n.2899C>G
ENST00000636254.1:n.356C>G
ENST00000636930.2:c.4436C>G MANE Select	ENSP00000490491.2:p.Pro1479Arg
ENST00000636940.1:n.2433C>G
ENST00000637015.1:c.1804C>G
ENST00000637568.1:c.1718C>G
ENST00000637741.1:n.1102C>G
ENST00000637810.1:c.1778C>G	ENSP00000489636.1:p.Pro593Arg
ENST00000637904.1:c.1937C>G	ENSP00000490550.1:p.Pro646Arg
ENST00000647938.1:c.4067C>G	ENSP00000498155.1:p.Pro1356Arg
ENST00000346085.9:c.4067C>G	ENSP00000344546.4:p.Pro1356Arg
ENST00000350026.9:c.4028C>G	ENSP00000055163.7:p.Pro1343Arg
ENST00000414678.6:c.2594C>G	ENSP00000412835.2:p.Pro865Arg
NM_017519.2:c.4028C>G	NP_059989.2:p.Pro1343Arg
NM_020732.3:c.4067C>G	NP_065783.3:p.Pro1356Arg
XM_005267069.3:c.4187C>G	XP_005267126.2:p.Pro1396Arg
XM_011535984.1:c.3266C>G	XP_011534286.1:p.Pro1089Arg
XM_011535985.1:c.3086C>G	XP_011534287.1:p.Pro1029Arg
XM_011535986.1:c.2846C>G	XP_011534288.1:p.Pro949Arg
XM_011535987.1:c.2465C>G	XP_011534289.1:p.Pro822Arg
XM_011535988.1:c.1328C>G	XP_011534290.1:p.Pro443Arg
NM_001346813.1:c.4187C>G	NP_001333742.1:p.Pro1396Arg
NM_001363725.1:c.1937C>G	NP_001350654.1:p.Pro646Arg
XM_011535984.2:c.4397C>G	XP_011534286.2:p.Pro1466Arg
XM_011535988.3:c.1328C>G	XP_011534290.1:p.Pro443Arg
XM_017011103.2:c.4298C>G	XP_016866592.1:p.Pro1433Arg
XM_017011104.1:c.4268C>G	XP_016866593.1:p.Pro1423Arg
XM_017011105.2:c.4238C>G	XP_016866594.1:p.Pro1413Arg
XM_017011106.2:c.4109C>G	XP_016866595.1:p.Pro1370Arg
XM_017011107.2:c.4088C>G	XP_016866596.1:p.Pro1363Arg
XR_002956289.1:n.4427-1841C>G
NM_001363725.2:c.1937C>G	NP_001350654.1:p.Pro646Arg
NM_001371656.1:c.4316C>G	NP_001358585.1:p.Pro1439Arg
NM_001374820.1:c.4316C>G	NP_001361749.1:p.Pro1439Arg
NM_001374828.1:c.4436C>G MANE Select	NP_001361757.1:p.Pro1479Arg
NM_017519.3:c.4277C>G	NP_059989.3:p.Pro1426Arg