Canonical Allele Identifier: CA366242674

Gene: ARID1B

Linked Data

• dbSNP Id: rs1168651010
• MyVariant Identifiers: chr6:g.157522481C>G (hg19) ; chr6:g.157201347C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201347C>G , CM000668.2:g.157201347C>G	GRCh38
NC_000006.11:g.157522481C>G , CM000668.1:g.157522481C>G	GRCh37
NC_000006.10:g.157564173C>G	NCBI36
NG_032093.1:g.428418C>G
NG_032093.2:g.428418C>G
NG_066624.1:g.430322C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4963C>G	ENSP00000055163.8:p.Pro1655Ala
ENST00000414678.8:c.5032C>G	ENSP00000412835.3:p.Pro1678Ala
ENST00000637015.2:c.5251C>G	ENSP00000489729.2:p.Pro1751Ala
ENST00000346085.10:c.5002C>G	ENSP00000344546.5:p.Pro1668Ala
ENST00000350026.10:c.4714C>G	ENSP00000055163.7:p.Pro1572Ala
ENST00000414678.7:c.3280C>G	ENSP00000412835.2:p.Pro1094Ala
ENST00000635849.1:c.2443C>G	ENSP00000490948.1:p.Pro815Ala
ENST00000635957.1:c.2074C>G	ENSP00000490385.1:p.Pro692Ala
ENST00000636227.1:n.3585C>G
ENST00000636254.1:n.1042C>G
ENST00000636930.2:c.5122C>G MANE Select	ENSP00000490491.2:p.Pro1708Ala
ENST00000636940.1:n.3119C>G
ENST00000637015.1:c.2490C>G
ENST00000637568.1:c.2404C>G
ENST00000637741.1:n.1788C>G
ENST00000637810.1:c.2464C>G	ENSP00000489636.1:p.Pro822Ala
ENST00000637904.1:c.2623C>G	ENSP00000490550.1:p.Pro875Ala
ENST00000647938.1:c.4753C>G	ENSP00000498155.1:p.Pro1585Ala
ENST00000346085.9:c.4753C>G	ENSP00000344546.4:p.Pro1585Ala
ENST00000350026.9:c.4714C>G	ENSP00000055163.7:p.Pro1572Ala
ENST00000414678.6:c.3280C>G	ENSP00000412835.2:p.Pro1094Ala
NM_017519.2:c.4714C>G	NP_059989.2:p.Pro1572Ala
NM_020732.3:c.4753C>G	NP_065783.3:p.Pro1585Ala
XM_005267069.3:c.4873C>G	XP_005267126.2:p.Pro1625Ala
XM_011535984.1:c.3952C>G	XP_011534286.1:p.Pro1318Ala
XM_011535985.1:c.3772C>G	XP_011534287.1:p.Pro1258Ala
XM_011535986.1:c.3532C>G	XP_011534288.1:p.Pro1178Ala
XM_011535987.1:c.3151C>G	XP_011534289.1:p.Pro1051Ala
XM_011535988.1:c.2014C>G	XP_011534290.1:p.Pro672Ala
NM_001346813.1:c.4873C>G	NP_001333742.1:p.Pro1625Ala
NM_001363725.1:c.2623C>G	NP_001350654.1:p.Pro875Ala
XM_011535984.2:c.5083C>G	XP_011534286.2:p.Pro1695Ala
XM_011535988.3:c.2014C>G	XP_011534290.1:p.Pro672Ala
XM_017011103.2:c.4984C>G	XP_016866592.1:p.Pro1662Ala
XM_017011104.1:c.4954C>G	XP_016866593.1:p.Pro1652Ala
XM_017011105.2:c.4924C>G	XP_016866594.1:p.Pro1642Ala
XM_017011106.2:c.4795C>G	XP_016866595.1:p.Pro1599Ala
XM_017011107.2:c.4774C>G	XP_016866596.1:p.Pro1592Ala
XR_002956289.1:n.5069C>G
NM_001363725.2:c.2623C>G	NP_001350654.1:p.Pro875Ala
NM_001371656.1:c.5002C>G	NP_001358585.1:p.Pro1668Ala
NM_001374820.1:c.5002C>G	NP_001361749.1:p.Pro1668Ala
NM_001374828.1:c.5122C>G MANE Select	NP_001361757.1:p.Pro1708Ala
NM_017519.3:c.4963C>G	NP_059989.3:p.Pro1655Ala