Canonical Allele Identifier: CA4067025

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2814009
• ClinVar RCV Id: RCV003680732
• dbSNP Id: rs551597753
• ExAC: 6:157405906 G / A
• gnomAD v2: 6-157405906-G-A
• gnomAD v3: 6-157084772-G-A
• gnomAD v4: 6-157084772-G-A
• MyVariant Identifiers: chr6:g.157405906G>A (hg19) ; chr6:g.157084772G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084772G>A , CM000668.2:g.157084772G>A	GRCh38
NC_000006.11:g.157405906G>A , CM000668.1:g.157405906G>A	GRCh37
NC_000006.10:g.157447598G>A	NCBI36
NG_032093.1:g.311843G>A
NG_032093.2:g.311843G>A
NG_066624.1:g.313747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2358G>A	ENSP00000055163.8:p.Ala786=
ENST00000414678.8:c.2358G>A	ENSP00000412835.3:p.Ala786=
ENST00000637015.2:c.2358G>A	ENSP00000489729.2:p.Ala786=
ENST00000319584.11:c.372G>A	ENSP00000313006.7:p.Ala124=
ENST00000346085.10:c.2397G>A	ENSP00000344546.5:p.Ala799=
ENST00000350026.10:c.2109G>A	ENSP00000055163.7:p.Ala703=
ENST00000414678.7:c.606G>A	ENSP00000412835.2:p.Ala202=
ENST00000452544.2:n.259G>A
ENST00000493658.2:n.7G>A
ENST00000635849.1:c.-142G>A	ENSP00000490948.1:n.-142G>A
ENST00000636930.2:c.2358G>A MANE Select	ENSP00000490491.2:p.Ala786=
ENST00000637003.1:c.-142G>A	ENSP00000489666.1:n.-142G>A
ENST00000637810.1:c.-142G>A	ENSP00000489636.1:n.-142G>A
ENST00000637904.1:c.-142G>A	ENSP00000490550.1:n.-142G>A
ENST00000647938.1:c.2148G>A	ENSP00000498155.1:p.Ala716=
ENST00000674190.1:n.1107G>A
ENST00000319584.10:c.375G>A	ENSP00000313006.6:p.Ala125=
ENST00000346085.9:c.2148G>A	ENSP00000344546.4:p.Ala716=
ENST00000350026.9:c.2109G>A	ENSP00000055163.7:p.Ala703=
ENST00000414678.6:c.606G>A	ENSP00000412835.2:p.Ala202=
ENST00000452544.1:n.217G>A
ENST00000493658.1:n.7G>A
NM_017519.2:c.2109G>A	NP_059989.2:p.Ala703=
NM_020732.3:c.2148G>A	NP_065783.3:p.Ala716=
XM_005267069.3:c.2109G>A	XP_005267126.2:p.Ala703=
XM_011535984.1:c.1059G>A	XP_011534286.1:p.Ala353=
XM_011535985.1:c.1059G>A	XP_011534287.1:p.Ala353=
XM_011535986.1:c.639G>A	XP_011534288.1:p.Ala213=
XM_011535987.1:c.258G>A	XP_011534289.1:p.Ala86=
NM_001346813.1:c.2109G>A	NP_001333742.1:p.Ala703=
NM_001363725.1:c.-142G>A	NP_001350654.1:n.-142G>A
XM_011535984.2:c.2190G>A	XP_011534286.2:p.Ala730=
XM_017011103.2:c.2190G>A	XP_016866592.1:p.Ala730=
XM_017011104.1:c.2190G>A	XP_016866593.1:p.Ala730=
XM_017011105.2:c.2190G>A	XP_016866594.1:p.Ala730=
XM_017011106.2:c.2190G>A	XP_016866595.1:p.Ala730=
XM_017011107.2:c.2190G>A	XP_016866596.1:p.Ala730=
XR_002956289.1:n.2273G>A
NM_001363725.2:c.-142G>A	NP_001350654.1:n.-142G>A
NM_001371656.1:c.2397G>A	NP_001358585.1:p.Ala799=
NM_001374820.1:c.2397G>A	NP_001361749.1:p.Ala799=
NM_001374828.1:c.2358G>A MANE Select	NP_001361757.1:p.Ala786=
NM_017519.3:c.2358G>A	NP_059989.3:p.Ala786=