Canonical Allele Identifier: CA366241110

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522002A>C (hg19) ; chr6:g.157200868A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200868A>C , CM000668.2:g.157200868A>C	GRCh38
NC_000006.11:g.157522002A>C , CM000668.1:g.157522002A>C	GRCh37
NC_000006.10:g.157563694A>C	NCBI36
NG_032093.1:g.427939A>C
NG_032093.2:g.427939A>C
NG_066624.1:g.429843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4484A>C	ENSP00000055163.8:p.Tyr1495Ser
ENST00000414678.8:c.4553A>C	ENSP00000412835.3:p.Tyr1518Ser
ENST00000637015.2:c.4772A>C	ENSP00000489729.2:p.Tyr1591Ser
ENST00000346085.10:c.4523A>C	ENSP00000344546.5:p.Tyr1508Ser
ENST00000350026.10:c.4235A>C	ENSP00000055163.7:p.Tyr1412Ser
ENST00000414678.7:c.2801A>C	ENSP00000412835.2:p.Tyr934Ser
ENST00000635849.1:c.1964A>C	ENSP00000490948.1:p.Tyr655Ser
ENST00000635957.1:c.1595A>C	ENSP00000490385.1:p.Tyr532Ser
ENST00000636227.1:n.3106A>C
ENST00000636254.1:n.563A>C
ENST00000636930.2:c.4643A>C MANE Select	ENSP00000490491.2:p.Tyr1548Ser
ENST00000636940.1:n.2640A>C
ENST00000637015.1:c.2011A>C
ENST00000637568.1:c.1925A>C
ENST00000637741.1:n.1309A>C
ENST00000637810.1:c.1985A>C	ENSP00000489636.1:p.Tyr662Ser
ENST00000637904.1:c.2144A>C	ENSP00000490550.1:p.Tyr715Ser
ENST00000647938.1:c.4274A>C	ENSP00000498155.1:p.Tyr1425Ser
ENST00000346085.9:c.4274A>C	ENSP00000344546.4:p.Tyr1425Ser
ENST00000350026.9:c.4235A>C	ENSP00000055163.7:p.Tyr1412Ser
ENST00000414678.6:c.2801A>C	ENSP00000412835.2:p.Tyr934Ser
NM_017519.2:c.4235A>C	NP_059989.2:p.Tyr1412Ser
NM_020732.3:c.4274A>C	NP_065783.3:p.Tyr1425Ser
XM_005267069.3:c.4394A>C	XP_005267126.2:p.Tyr1465Ser
XM_011535984.1:c.3473A>C	XP_011534286.1:p.Tyr1158Ser
XM_011535985.1:c.3293A>C	XP_011534287.1:p.Tyr1098Ser
XM_011535986.1:c.3053A>C	XP_011534288.1:p.Tyr1018Ser
XM_011535987.1:c.2672A>C	XP_011534289.1:p.Tyr891Ser
XM_011535988.1:c.1535A>C	XP_011534290.1:p.Tyr512Ser
NM_001346813.1:c.4394A>C	NP_001333742.1:p.Tyr1465Ser
NM_001363725.1:c.2144A>C	NP_001350654.1:p.Tyr715Ser
XM_011535984.2:c.4604A>C	XP_011534286.2:p.Tyr1535Ser
XM_011535988.3:c.1535A>C	XP_011534290.1:p.Tyr512Ser
XM_017011103.2:c.4505A>C	XP_016866592.1:p.Tyr1502Ser
XM_017011104.1:c.4475A>C	XP_016866593.1:p.Tyr1492Ser
XM_017011105.2:c.4445A>C	XP_016866594.1:p.Tyr1482Ser
XM_017011106.2:c.4316A>C	XP_016866595.1:p.Tyr1439Ser
XM_017011107.2:c.4295A>C	XP_016866596.1:p.Tyr1432Ser
XR_002956289.1:n.4590A>C
NM_001363725.2:c.2144A>C	NP_001350654.1:p.Tyr715Ser
NM_001371656.1:c.4523A>C	NP_001358585.1:p.Tyr1508Ser
NM_001374820.1:c.4523A>C	NP_001361749.1:p.Tyr1508Ser
NM_001374828.1:c.4643A>C MANE Select	NP_001361757.1:p.Tyr1548Ser
NM_017519.3:c.4484A>C	NP_059989.3:p.Tyr1495Ser