Canonical Allele Identifier: CA366242785

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376307
• MyVariant Identifiers: chr6:g.157522503T>G (hg19) ; chr6:g.157201369T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201369T>G , CM000668.2:g.157201369T>G	GRCh38
NC_000006.11:g.157522503T>G , CM000668.1:g.157522503T>G	GRCh37
NC_000006.10:g.157564195T>G	NCBI36
NG_032093.1:g.428440T>G
NG_032093.2:g.428440T>G
NG_066624.1:g.430344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4985T>G	ENSP00000055163.8:p.Val1662Gly
ENST00000414678.8:c.5054T>G	ENSP00000412835.3:p.Val1685Gly
ENST00000637015.2:c.5273T>G	ENSP00000489729.2:p.Val1758Gly
ENST00000346085.10:c.5024T>G	ENSP00000344546.5:p.Val1675Gly
ENST00000350026.10:c.4736T>G	ENSP00000055163.7:p.Val1579Gly
ENST00000414678.7:c.3302T>G	ENSP00000412835.2:p.Val1101Gly
ENST00000635849.1:c.2465T>G	ENSP00000490948.1:p.Val822Gly
ENST00000635957.1:c.2096T>G	ENSP00000490385.1:p.Val699Gly
ENST00000636227.1:n.3607T>G
ENST00000636254.1:n.1064T>G
ENST00000636930.2:c.5144T>G MANE Select	ENSP00000490491.2:p.Val1715Gly
ENST00000636940.1:n.3141T>G
ENST00000637015.1:c.2512T>G
ENST00000637568.1:c.2426T>G
ENST00000637741.1:n.1810T>G
ENST00000637810.1:c.2486T>G	ENSP00000489636.1:p.Val829Gly
ENST00000637904.1:c.2645T>G	ENSP00000490550.1:p.Val882Gly
ENST00000647938.1:c.4775T>G	ENSP00000498155.1:p.Val1592Gly
ENST00000346085.9:c.4775T>G	ENSP00000344546.4:p.Val1592Gly
ENST00000350026.9:c.4736T>G	ENSP00000055163.7:p.Val1579Gly
ENST00000414678.6:c.3302T>G	ENSP00000412835.2:p.Val1101Gly
NM_017519.2:c.4736T>G	NP_059989.2:p.Val1579Gly
NM_020732.3:c.4775T>G	NP_065783.3:p.Val1592Gly
XM_005267069.3:c.4895T>G	XP_005267126.2:p.Val1632Gly
XM_011535984.1:c.3974T>G	XP_011534286.1:p.Val1325Gly
XM_011535985.1:c.3794T>G	XP_011534287.1:p.Val1265Gly
XM_011535986.1:c.3554T>G	XP_011534288.1:p.Val1185Gly
XM_011535987.1:c.3173T>G	XP_011534289.1:p.Val1058Gly
XM_011535988.1:c.2036T>G	XP_011534290.1:p.Val679Gly
NM_001346813.1:c.4895T>G	NP_001333742.1:p.Val1632Gly
NM_001363725.1:c.2645T>G	NP_001350654.1:p.Val882Gly
XM_011535984.2:c.5105T>G	XP_011534286.2:p.Val1702Gly
XM_011535988.3:c.2036T>G	XP_011534290.1:p.Val679Gly
XM_017011103.2:c.5006T>G	XP_016866592.1:p.Val1669Gly
XM_017011104.1:c.4976T>G	XP_016866593.1:p.Val1659Gly
XM_017011105.2:c.4946T>G	XP_016866594.1:p.Val1649Gly
XM_017011106.2:c.4817T>G	XP_016866595.1:p.Val1606Gly
XM_017011107.2:c.4796T>G	XP_016866596.1:p.Val1599Gly
XR_002956289.1:n.5091T>G
NM_001363725.2:c.2645T>G	NP_001350654.1:p.Val882Gly
NM_001371656.1:c.5024T>G	NP_001358585.1:p.Val1675Gly
NM_001374820.1:c.5024T>G	NP_001361749.1:p.Val1675Gly
NM_001374828.1:c.5144T>G MANE Select	NP_001361757.1:p.Val1715Gly
NM_017519.3:c.4985T>G	NP_059989.3:p.Val1662Gly