Canonical Allele Identifier: CA366242783

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4985T>C	ENSP00000055163.8:p.Val1662Ala
ENST00000414678.8:c.5054T>C	ENSP00000412835.3:p.Val1685Ala
ENST00000637015.2:c.5273T>C	ENSP00000489729.2:p.Val1758Ala
ENST00000346085.10:c.5024T>C	ENSP00000344546.5:p.Val1675Ala
ENST00000350026.10:c.4736T>C	ENSP00000055163.7:p.Val1579Ala
ENST00000414678.7:c.3302T>C	ENSP00000412835.2:p.Val1101Ala
ENST00000635849.1:c.2465T>C	ENSP00000490948.1:p.Val822Ala
ENST00000635957.1:c.2096T>C	ENSP00000490385.1:p.Val699Ala
ENST00000636227.1:n.3607T>C
ENST00000636254.1:n.1064T>C
ENST00000636930.2:c.5144T>C MANE Select	ENSP00000490491.2:p.Val1715Ala
ENST00000636940.1:n.3141T>C
ENST00000637015.1:c.2512T>C
ENST00000637568.1:c.2426T>C
ENST00000637741.1:n.1810T>C
ENST00000637810.1:c.2486T>C	ENSP00000489636.1:p.Val829Ala
ENST00000637904.1:c.2645T>C	ENSP00000490550.1:p.Val882Ala
ENST00000647938.1:c.4775T>C	ENSP00000498155.1:p.Val1592Ala
ENST00000346085.9:c.4775T>C	ENSP00000344546.4:p.Val1592Ala
ENST00000350026.9:c.4736T>C	ENSP00000055163.7:p.Val1579Ala
ENST00000414678.6:c.3302T>C	ENSP00000412835.2:p.Val1101Ala
NM_017519.2:c.4736T>C	NP_059989.2:p.Val1579Ala
NM_020732.3:c.4775T>C	NP_065783.3:p.Val1592Ala
XM_005267069.3:c.4895T>C	XP_005267126.2:p.Val1632Ala
XM_011535984.1:c.3974T>C	XP_011534286.1:p.Val1325Ala
XM_011535985.1:c.3794T>C	XP_011534287.1:p.Val1265Ala
XM_011535986.1:c.3554T>C	XP_011534288.1:p.Val1185Ala
XM_011535987.1:c.3173T>C	XP_011534289.1:p.Val1058Ala
XM_011535988.1:c.2036T>C	XP_011534290.1:p.Val679Ala
NM_001346813.1:c.4895T>C	NP_001333742.1:p.Val1632Ala
NM_001363725.1:c.2645T>C	NP_001350654.1:p.Val882Ala
XM_011535984.2:c.5105T>C	XP_011534286.2:p.Val1702Ala
XM_011535988.3:c.2036T>C	XP_011534290.1:p.Val679Ala
XM_017011103.2:c.5006T>C	XP_016866592.1:p.Val1669Ala
XM_017011104.1:c.4976T>C	XP_016866593.1:p.Val1659Ala
XM_017011105.2:c.4946T>C	XP_016866594.1:p.Val1649Ala
XM_017011106.2:c.4817T>C	XP_016866595.1:p.Val1606Ala
XM_017011107.2:c.4796T>C	XP_016866596.1:p.Val1599Ala
XR_002956289.1:n.5091T>C
NM_001363725.2:c.2645T>C	NP_001350654.1:p.Val882Ala
NM_001371656.1:c.5024T>C	NP_001358585.1:p.Val1675Ala
NM_001374820.1:c.5024T>C	NP_001361749.1:p.Val1675Ala
NM_001374828.1:c.5144T>C MANE Select	NP_001361757.1:p.Val1715Ala
NM_017519.3:c.4985T>C	NP_059989.3:p.Val1662Ala