Canonical Allele Identifier: CA4067366

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2045226
• ClinVar RCV Id: RCV002918024
• dbSNP Id: rs778366844
• ExAC: 6:157502246 G / A
• gnomAD v2: 6-157502246-G-A
• gnomAD v4: 6-157181112-G-A
• MyVariant Identifiers: chr6:g.157502246G>A (hg19) ; chr6:g.157181112G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181112G>A , CM000668.2:g.157181112G>A	GRCh38
NC_000006.11:g.157502246G>A , CM000668.1:g.157502246G>A	GRCh37
NC_000006.10:g.157543938G>A	NCBI36
NG_032093.1:g.408183G>A
NG_032093.2:g.408183G>A
NG_066624.1:g.410087G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3489G>A	ENSP00000055163.8:p.Val1163=
ENST00000414678.8:c.3558G>A	ENSP00000412835.3:p.Val1186=
ENST00000637015.2:c.3777G>A	ENSP00000489729.2:p.Val1259=
ENST00000319584.11:c.1662G>A	ENSP00000313006.7:p.Val554=
ENST00000346085.10:c.3528G>A	ENSP00000344546.5:p.Val1176=
ENST00000350026.10:c.3240G>A	ENSP00000055163.7:p.Val1080=
ENST00000414678.7:c.1806G>A	ENSP00000412835.2:p.Val602=
ENST00000635849.1:c.969G>A	ENSP00000490948.1:p.Val323=
ENST00000635957.1:c.603G>A	ENSP00000490385.1:p.Val201=
ENST00000636930.2:c.3648G>A MANE Select	ENSP00000490491.2:p.Val1216=
ENST00000636940.1:n.1645G>A
ENST00000637015.1:c.1016G>A
ENST00000637568.1:c.930G>A
ENST00000637741.1:n.314G>A
ENST00000637810.1:c.990G>A	ENSP00000489636.1:p.Val330=
ENST00000637904.1:c.1149G>A	ENSP00000490550.1:p.Val383=
ENST00000647938.1:c.3279G>A	ENSP00000498155.1:p.Val1093=
ENST00000319584.10:c.1665G>A	ENSP00000313006.6:p.Val555=
ENST00000346085.9:c.3279G>A	ENSP00000344546.4:p.Val1093=
ENST00000350026.9:c.3240G>A	ENSP00000055163.7:p.Val1080=
ENST00000400790.3:c.441G>A	ENSP00000383596.3:p.Val147=
ENST00000414678.6:c.1806G>A	ENSP00000412835.2:p.Val602=
ENST00000478761.3:c.850G>A
NM_017519.2:c.3240G>A	NP_059989.2:p.Val1080=
NM_020732.3:c.3279G>A	NP_065783.3:p.Val1093=
XM_005267069.3:c.3399G>A	XP_005267126.2:p.Val1133=
XM_011535984.1:c.2478G>A	XP_011534286.1:p.Val826=
XM_011535985.1:c.2298G>A	XP_011534287.1:p.Val766=
XM_011535986.1:c.2058G>A	XP_011534288.1:p.Val686=
XM_011535987.1:c.1677G>A	XP_011534289.1:p.Val559=
XM_011535988.1:c.540G>A	XP_011534290.1:p.Val180=
NM_001346813.1:c.3399G>A	NP_001333742.1:p.Val1133=
NM_001363725.1:c.1149G>A	NP_001350654.1:p.Val383=
XM_011535984.2:c.3609G>A	XP_011534286.2:p.Val1203=
XM_011535988.3:c.540G>A	XP_011534290.1:p.Val180=
XM_017011103.2:c.3510G>A	XP_016866592.1:p.Val1170=
XM_017011104.1:c.3480G>A	XP_016866593.1:p.Val1160=
XM_017011105.2:c.3450G>A	XP_016866594.1:p.Val1150=
XM_017011106.2:c.3321G>A	XP_016866595.1:p.Val1107=
XM_017011107.2:c.3300G>A	XP_016866596.1:p.Val1100=
XR_002956289.1:n.3692G>A
NM_001363725.2:c.1149G>A	NP_001350654.1:p.Val383=
NM_001371656.1:c.3528G>A	NP_001358585.1:p.Val1176=
NM_001374820.1:c.3528G>A	NP_001361749.1:p.Val1176=
NM_001374828.1:c.3648G>A MANE Select	NP_001361757.1:p.Val1216=
NM_017519.3:c.3489G>A	NP_059989.3:p.Val1163=