Canonical Allele Identifier: CA366389297

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470079A>T (hg19) ; chr6:g.157148945A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148945A>T , CM000668.2:g.157148945A>T	GRCh38
NC_000006.11:g.157470079A>T , CM000668.1:g.157470079A>T	GRCh37
NC_000006.10:g.157511771A>T	NCBI36
NG_032093.1:g.376016A>T
NG_032093.2:g.376016A>T
NG_066624.1:g.377920A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3083A>T	ENSP00000055163.8:p.Gln1028Leu
ENST00000414678.8:c.2993A>T	ENSP00000412835.3:p.Gln998Leu
ENST00000637015.2:c.3083A>T	ENSP00000489729.2:p.Gln1028Leu
ENST00000319584.11:c.1097A>T	ENSP00000313006.7:p.Gln366Leu
ENST00000346085.10:c.3122A>T	ENSP00000344546.5:p.Gln1041Leu
ENST00000350026.10:c.2834A>T	ENSP00000055163.7:p.Gln945Leu
ENST00000414678.7:c.1241A>T	ENSP00000412835.2:p.Gln414Leu
ENST00000452544.2:n.984A>T
ENST00000635849.1:c.404A>T	ENSP00000490948.1:p.Gln135Leu
ENST00000635957.1:c.38A>T	ENSP00000490385.1:p.Gln13Leu
ENST00000636426.1:n.217A>T
ENST00000636930.2:c.3083A>T MANE Select	ENSP00000490491.2:p.Gln1028Leu
ENST00000637015.1:c.322A>T
ENST00000637568.1:c.126A>T
ENST00000637810.1:c.584A>T	ENSP00000489636.1:p.Gln195Leu
ENST00000637904.1:c.584A>T	ENSP00000490550.1:p.Gln195Leu
ENST00000647938.1:c.2873A>T	ENSP00000498155.1:p.Gln958Leu
ENST00000674190.1:n.1832A>T
ENST00000319584.10:c.1100A>T	ENSP00000313006.6:p.Gln367Leu
ENST00000346085.9:c.2873A>T	ENSP00000344546.4:p.Gln958Leu
ENST00000350026.9:c.2834A>T	ENSP00000055163.7:p.Gln945Leu
ENST00000400790.3:c.35A>T	ENSP00000383596.3:p.Gln12Leu
ENST00000414678.6:c.1241A>T	ENSP00000412835.2:p.Gln414Leu
ENST00000452544.1:n.930A>T
ENST00000478761.3:c.156A>T
NM_017519.2:c.2834A>T	NP_059989.2:p.Gln945Leu
NM_020732.3:c.2873A>T	NP_065783.3:p.Gln958Leu
XM_005267069.3:c.2834A>T	XP_005267126.2:p.Gln945Leu
XM_011535984.1:c.1784A>T	XP_011534286.1:p.Gln595Leu
XM_011535985.1:c.1604A>T	XP_011534287.1:p.Gln535Leu
XM_011535986.1:c.1364A>T	XP_011534288.1:p.Gln455Leu
XM_011535987.1:c.983A>T	XP_011534289.1:p.Gln328Leu
XM_011535988.1:c.-20+15738A>T	XP_011534290.1:n.-20+15738A>T
NM_001346813.1:c.2834A>T	NP_001333742.1:p.Gln945Leu
NM_001363725.1:c.584A>T	NP_001350654.1:p.Gln195Leu
XM_011535984.2:c.2915A>T	XP_011534286.2:p.Gln972Leu
XM_011535988.3:c.-20+15738A>T	XP_011534290.1:n.-20+15738A>T
XM_017011103.2:c.2915A>T	XP_016866592.1:p.Gln972Leu
XM_017011104.1:c.2915A>T	XP_016866593.1:p.Gln972Leu
XM_017011105.2:c.2915A>T	XP_016866594.1:p.Gln972Leu
XM_017011106.2:c.2915A>T	XP_016866595.1:p.Gln972Leu
XM_017011107.2:c.2735A>T	XP_016866596.1:p.Gln912Leu
XR_002956289.1:n.2998A>T
NM_001363725.2:c.584A>T	NP_001350654.1:p.Gln195Leu
NM_001371656.1:c.3122A>T	NP_001358585.1:p.Gln1041Leu
NM_001374820.1:c.3122A>T	NP_001361749.1:p.Gln1041Leu
NM_001374828.1:c.3083A>T MANE Select	NP_001361757.1:p.Gln1028Leu
NM_017519.3:c.3083A>T	NP_059989.3:p.Gln1028Leu