Canonical Allele Identifier: CA366389651

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157167187T>A , CM000668.2:g.157167187T>A	GRCh38
NC_000006.11:g.157488321T>A , CM000668.1:g.157488321T>A	GRCh37
NC_000006.10:g.157530013T>A	NCBI36
NG_032093.1:g.394258T>A
NG_032093.2:g.394258T>A
NG_066624.1:g.396162T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.3235+2T>A MANE Select	NP_001361757.1:n.3235+2T>A
ENST00000636930.2:c.3235+2T>A MANE Select	ENSP00000490491.2:n.3235+2T>A
NM_001346813.1:c.2986+2T>A	NP_001333742.1:n.2986+2T>A
NM_001363725.1:c.736+2T>A	NP_001350654.1:n.736+2T>A
NM_001363725.2:c.736+2T>A	NP_001350654.1:n.736+2T>A
NM_001371656.1:c.3274+2T>A	NP_001358585.1:n.3274+2T>A
NM_001374820.1:c.3274+2T>A	NP_001361749.1:n.3274+2T>A
NM_017519.2:c.2986+2T>A	NP_059989.2:n.2986+2T>A
NM_017519.3:c.3235+2T>A	NP_059989.3:n.3235+2T>A
NM_020732.3:c.3025+2T>A	NP_065783.3:n.3025+2T>A
ENST00000319584.10:c.1252+2T>A	ENSP00000313006.6:n.1252+2T>A
ENST00000319584.11:c.1249+2T>A	ENSP00000313006.7:n.1249+2T>A
ENST00000346085.10:c.3274+2T>A	ENSP00000344546.5:n.3274+2T>A
ENST00000346085.9:c.3025+2T>A	ENSP00000344546.4:n.3025+2T>A
ENST00000350026.10:c.2986+2T>A	ENSP00000055163.7:n.2986+2T>A
ENST00000350026.11:c.3235+2T>A	ENSP00000055163.8:n.3235+2T>A
ENST00000350026.9:c.2986+2T>A	ENSP00000055163.7:n.2986+2T>A
ENST00000400790.3:c.187+2T>A	ENSP00000383596.3:n.187+2T>A
ENST00000414678.6:c.1393+2T>A	ENSP00000412835.2:n.1393+2T>A
ENST00000414678.7:c.1393+2T>A	ENSP00000412835.2:n.1393+2T>A
ENST00000414678.8:c.3145+2T>A	ENSP00000412835.3:n.3145+2T>A
ENST00000478761.3:c.437+2T>A
ENST00000635849.1:c.556+2T>A	ENSP00000490948.1:n.556+2T>A
ENST00000635957.1:c.190+2T>A	ENSP00000490385.1:n.190+2T>A
ENST00000636426.1:n.401T>A
ENST00000637015.1:c.603+2T>A
ENST00000637015.2:c.3364+2T>A	ENSP00000489729.2:n.3364+2T>A
ENST00000637568.1:c.517+2T>A
ENST00000637722.1:n.1173T>A
ENST00000637810.1:c.736+2T>A	ENSP00000489636.1:n.736+2T>A
ENST00000637904.1:c.736+2T>A	ENSP00000490550.1:n.736+2T>A
ENST00000647938.1:c.3025+2T>A	ENSP00000498155.1:n.3025+2T>A
XM_005267069.3:c.2986+2T>A	XP_005267126.2:n.2986+2T>A
XM_011535984.1:c.2065+2T>A	XP_011534286.1:n.2065+2T>A
XM_011535984.2:c.3196+2T>A	XP_011534286.2:n.3196+2T>A
XM_011535985.1:c.1885+2T>A	XP_011534287.1:n.1885+2T>A
XM_011535986.1:c.1645+2T>A	XP_011534288.1:n.1645+2T>A
XM_011535987.1:c.1264+2T>A	XP_011534289.1:n.1264+2T>A
XM_011535988.1:c.127+2T>A	XP_011534290.1:n.127+2T>A
XM_011535988.3:c.127+2T>A	XP_011534290.1:n.127+2T>A
XM_017011103.2:c.3097+2T>A	XP_016866592.1:n.3097+2T>A
XM_017011104.1:c.3067+2T>A	XP_016866593.1:n.3067+2T>A
XM_017011105.2:c.3196+2T>A	XP_016866594.1:n.3196+2T>A
XM_017011106.2:c.3067+2T>A	XP_016866595.1:n.3067+2T>A
XM_017011107.2:c.2887+2T>A	XP_016866596.1:n.2887+2T>A
XR_002956289.1:n.3279+2T>A