Canonical Allele Identifier: CA366381020

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157222659G>T (hg19) ; chr6:g.156901525G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901525G>T , CM000668.2:g.156901525G>T	GRCh38
NC_000006.11:g.157222659G>T , CM000668.1:g.157222659G>T	GRCh37
NC_000006.10:g.157264351G>T	NCBI36
NG_032093.1:g.128596G>T
NG_032093.2:g.128596G>T
NG_066624.1:g.130500G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2136G>T	ENSP00000055163.8:p.Gln712His
ENST00000414678.8:c.2136G>T	ENSP00000412835.3:p.Gln712His
ENST00000637015.2:c.2136G>T	ENSP00000489729.2:p.Gln712His
ENST00000319584.11:c.150G>T	ENSP00000313006.7:p.Gln50His
ENST00000346085.10:c.2175G>T	ENSP00000344546.5:p.Gln725His
ENST00000350026.10:c.1887G>T	ENSP00000055163.7:p.Gln629His
ENST00000414678.7:c.384G>T	ENSP00000412835.2:p.Gln128His
ENST00000636205.1:n.199G>T
ENST00000636748.1:c.417G>T	ENSP00000489917.1:p.Gln139His
ENST00000636930.2:c.2136G>T MANE Select	ENSP00000490491.2:p.Gln712His
ENST00000637532.1:c.162G>T	ENSP00000490420.1:p.Gln54His
ENST00000638000.1:c.353G>T
ENST00000647938.1:c.1926G>T	ENSP00000498155.1:p.Gln642His
ENST00000674190.1:n.843G>T
ENST00000674298.1:c.1876G>T
ENST00000319584.10:c.153G>T	ENSP00000313006.6:p.Gln51His
ENST00000346085.9:c.1926G>T	ENSP00000344546.4:p.Gln642His
ENST00000350026.9:c.1887G>T	ENSP00000055163.7:p.Gln629His
ENST00000414678.6:c.384G>T	ENSP00000412835.2:p.Gln128His
NM_017519.2:c.1887G>T	NP_059989.2:p.Gln629His
NM_020732.3:c.1926G>T	NP_065783.3:p.Gln642His
XM_005267069.3:c.1887G>T	XP_005267126.2:p.Gln629His
XM_011535984.1:c.795G>T	XP_011534286.1:p.Gln265His
XM_011535985.1:c.795G>T	XP_011534287.1:p.Gln265His
XM_011535986.1:c.375G>T	XP_011534288.1:p.Gln125His
NM_001346813.1:c.1887G>T	NP_001333742.1:p.Gln629His
XM_011535984.2:c.1926G>T	XP_011534286.2:p.Gln642His
XM_017011103.2:c.1926G>T	XP_016866592.1:p.Gln642His
XM_017011104.1:c.1926G>T	XP_016866593.1:p.Gln642His
XM_017011105.2:c.1926G>T	XP_016866594.1:p.Gln642His
XM_017011106.2:c.1926G>T	XP_016866595.1:p.Gln642His
XM_017011107.2:c.1926G>T	XP_016866596.1:p.Gln642His
XR_002956289.1:n.2009G>T
NM_001371656.1:c.2175G>T	NP_001358585.1:p.Gln725His
NM_001374820.1:c.2175G>T	NP_001361749.1:p.Gln725His
NM_001374828.1:c.2136G>T MANE Select	NP_001361757.1:p.Gln712His
NM_017519.3:c.2136G>T	NP_059989.3:p.Gln712His