Canonical Allele Identifier: CA366241124

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522008A>T (hg19) ; chr6:g.157200874A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200874A>T , CM000668.2:g.157200874A>T	GRCh38
NC_000006.11:g.157522008A>T , CM000668.1:g.157522008A>T	GRCh37
NC_000006.10:g.157563700A>T	NCBI36
NG_032093.1:g.427945A>T
NG_032093.2:g.427945A>T
NG_066624.1:g.429849A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4490A>T	ENSP00000055163.8:p.Tyr1497Phe
ENST00000414678.8:c.4559A>T	ENSP00000412835.3:p.Tyr1520Phe
ENST00000637015.2:c.4778A>T	ENSP00000489729.2:p.Tyr1593Phe
ENST00000346085.10:c.4529A>T	ENSP00000344546.5:p.Tyr1510Phe
ENST00000350026.10:c.4241A>T	ENSP00000055163.7:p.Tyr1414Phe
ENST00000414678.7:c.2807A>T	ENSP00000412835.2:p.Tyr936Phe
ENST00000635849.1:c.1970A>T	ENSP00000490948.1:p.Tyr657Phe
ENST00000635957.1:c.1601A>T	ENSP00000490385.1:p.Tyr534Phe
ENST00000636227.1:n.3112A>T
ENST00000636254.1:n.569A>T
ENST00000636930.2:c.4649A>T MANE Select	ENSP00000490491.2:p.Tyr1550Phe
ENST00000636940.1:n.2646A>T
ENST00000637015.1:c.2017A>T
ENST00000637568.1:c.1931A>T
ENST00000637741.1:n.1315A>T
ENST00000637810.1:c.1991A>T	ENSP00000489636.1:p.Tyr664Phe
ENST00000637904.1:c.2150A>T	ENSP00000490550.1:p.Tyr717Phe
ENST00000647938.1:c.4280A>T	ENSP00000498155.1:p.Tyr1427Phe
ENST00000346085.9:c.4280A>T	ENSP00000344546.4:p.Tyr1427Phe
ENST00000350026.9:c.4241A>T	ENSP00000055163.7:p.Tyr1414Phe
ENST00000414678.6:c.2807A>T	ENSP00000412835.2:p.Tyr936Phe
NM_017519.2:c.4241A>T	NP_059989.2:p.Tyr1414Phe
NM_020732.3:c.4280A>T	NP_065783.3:p.Tyr1427Phe
XM_005267069.3:c.4400A>T	XP_005267126.2:p.Tyr1467Phe
XM_011535984.1:c.3479A>T	XP_011534286.1:p.Tyr1160Phe
XM_011535985.1:c.3299A>T	XP_011534287.1:p.Tyr1100Phe
XM_011535986.1:c.3059A>T	XP_011534288.1:p.Tyr1020Phe
XM_011535987.1:c.2678A>T	XP_011534289.1:p.Tyr893Phe
XM_011535988.1:c.1541A>T	XP_011534290.1:p.Tyr514Phe
NM_001346813.1:c.4400A>T	NP_001333742.1:p.Tyr1467Phe
NM_001363725.1:c.2150A>T	NP_001350654.1:p.Tyr717Phe
XM_011535984.2:c.4610A>T	XP_011534286.2:p.Tyr1537Phe
XM_011535988.3:c.1541A>T	XP_011534290.1:p.Tyr514Phe
XM_017011103.2:c.4511A>T	XP_016866592.1:p.Tyr1504Phe
XM_017011104.1:c.4481A>T	XP_016866593.1:p.Tyr1494Phe
XM_017011105.2:c.4451A>T	XP_016866594.1:p.Tyr1484Phe
XM_017011106.2:c.4322A>T	XP_016866595.1:p.Tyr1441Phe
XM_017011107.2:c.4301A>T	XP_016866596.1:p.Tyr1434Phe
XR_002956289.1:n.4596A>T
NM_001363725.2:c.2150A>T	NP_001350654.1:p.Tyr717Phe
NM_001371656.1:c.4529A>T	NP_001358585.1:p.Tyr1510Phe
NM_001374820.1:c.4529A>T	NP_001361749.1:p.Tyr1510Phe
NM_001374828.1:c.4649A>T MANE Select	NP_001361757.1:p.Tyr1550Phe
NM_017519.3:c.4490A>T	NP_059989.3:p.Tyr1497Phe