Canonical Allele Identifier: CA452989959

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128463309
• gnomAD v4: 6-157084874-A-T
• MyVariant Identifiers: chr6:g.157406008A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084874A>T , CM000668.2:g.157084874A>T	GRCh38
NC_000006.11:g.157406008A>T , CM000668.1:g.157406008A>T	GRCh37
NC_000006.10:g.157447700A>T	NCBI36
NG_032093.1:g.311945A>T
NG_032093.2:g.311945A>T
NG_066624.1:g.313849A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2460A>T	ENSP00000055163.8:p.Arg820=
ENST00000414678.8:c.2460A>T	ENSP00000412835.3:p.Arg820=
ENST00000637015.2:c.2460A>T	ENSP00000489729.2:p.Arg820=
ENST00000319584.11:c.474A>T	ENSP00000313006.7:p.Arg158=
ENST00000346085.10:c.2499A>T	ENSP00000344546.5:p.Arg833=
ENST00000350026.10:c.2211A>T	ENSP00000055163.7:p.Arg737=
ENST00000414678.7:c.708A>T	ENSP00000412835.2:p.Arg236=
ENST00000452544.2:n.361A>T
ENST00000493658.2:n.109A>T
ENST00000635849.1:c.-40A>T	ENSP00000490948.1:n.-40A>T
ENST00000636930.2:c.2460A>T MANE Select	ENSP00000490491.2:p.Arg820=
ENST00000637003.1:c.-40A>T	ENSP00000489666.1:n.-40A>T
ENST00000637810.1:c.-40A>T	ENSP00000489636.1:n.-40A>T
ENST00000637904.1:c.-40A>T	ENSP00000490550.1:n.-40A>T
ENST00000647938.1:c.2250A>T	ENSP00000498155.1:p.Arg750=
ENST00000674190.1:n.1209A>T
ENST00000319584.10:c.477A>T	ENSP00000313006.6:p.Arg159=
ENST00000346085.9:c.2250A>T	ENSP00000344546.4:p.Arg750=
ENST00000350026.9:c.2211A>T	ENSP00000055163.7:p.Arg737=
ENST00000414678.6:c.708A>T	ENSP00000412835.2:p.Arg236=
ENST00000452544.1:n.319A>T
ENST00000493658.1:n.109A>T
NM_017519.2:c.2211A>T	NP_059989.2:p.Arg737=
NM_020732.3:c.2250A>T	NP_065783.3:p.Arg750=
XM_005267069.3:c.2211A>T	XP_005267126.2:p.Arg737=
XM_011535984.1:c.1161A>T	XP_011534286.1:p.Arg387=
XM_011535985.1:c.1161A>T	XP_011534287.1:p.Arg387=
XM_011535986.1:c.741A>T	XP_011534288.1:p.Arg247=
XM_011535987.1:c.360A>T	XP_011534289.1:p.Arg120=
NM_001346813.1:c.2211A>T	NP_001333742.1:p.Arg737=
NM_001363725.1:c.-40A>T	NP_001350654.1:n.-40A>T
XM_011535984.2:c.2292A>T	XP_011534286.2:p.Arg764=
XM_017011103.2:c.2292A>T	XP_016866592.1:p.Arg764=
XM_017011104.1:c.2292A>T	XP_016866593.1:p.Arg764=
XM_017011105.2:c.2292A>T	XP_016866594.1:p.Arg764=
XM_017011106.2:c.2292A>T	XP_016866595.1:p.Arg764=
XM_017011107.2:c.2292A>T	XP_016866596.1:p.Arg764=
XR_002956289.1:n.2375A>T
NM_001363725.2:c.-40A>T	NP_001350654.1:n.-40A>T
NM_001371656.1:c.2499A>T	NP_001358585.1:p.Arg833=
NM_001374820.1:c.2499A>T	NP_001361749.1:p.Arg833=
NM_001374828.1:c.2460A>T MANE Select	NP_001361757.1:p.Arg820=
NM_017519.3:c.2460A>T	NP_059989.3:p.Arg820=