Canonical Allele Identifier: CA4067532

Gene: ARID1B

Linked Data

• dbSNP Id: rs747374301
• ExAC: 6:157511254 G / A
• gnomAD v2: 6-157511254-G-A
• gnomAD v3: 6-157190120-G-A
• gnomAD v4: 6-157190120-G-A
• MyVariant Identifiers: chr6:g.157511254G>A (hg19) ; chr6:g.157190120G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190120G>A , CM000668.2:g.157190120G>A	GRCh38
NC_000006.11:g.157511254G>A , CM000668.1:g.157511254G>A	GRCh37
NC_000006.10:g.157552946G>A	NCBI36
NG_032093.1:g.417191G>A
NG_032093.2:g.417191G>A
NG_066624.1:g.419095G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3982G>A	ENSP00000055163.8:p.Ala1328Thr
ENST00000414678.8:c.4051G>A	ENSP00000412835.3:p.Ala1351Thr
ENST00000637015.2:c.4270G>A	ENSP00000489729.2:p.Ala1424Thr
ENST00000346085.10:c.4021G>A	ENSP00000344546.5:p.Ala1341Thr
ENST00000350026.10:c.3733G>A	ENSP00000055163.7:p.Ala1245Thr
ENST00000414678.7:c.2299G>A	ENSP00000412835.2:p.Ala767Thr
ENST00000635849.1:c.1462G>A	ENSP00000490948.1:p.Ala488Thr
ENST00000635957.1:c.1093G>A	ENSP00000490385.1:p.Ala365Thr
ENST00000636930.2:c.4141G>A MANE Select	ENSP00000490491.2:p.Ala1381Thr
ENST00000636940.1:n.2138G>A
ENST00000637015.1:c.1509G>A
ENST00000637568.1:c.1423G>A
ENST00000637741.1:n.807G>A
ENST00000637810.1:c.1483G>A	ENSP00000489636.1:p.Ala495Thr
ENST00000637904.1:c.1642G>A	ENSP00000490550.1:p.Ala548Thr
ENST00000647938.1:c.3772G>A	ENSP00000498155.1:p.Ala1258Thr
ENST00000346085.9:c.3772G>A	ENSP00000344546.4:p.Ala1258Thr
ENST00000350026.9:c.3733G>A	ENSP00000055163.7:p.Ala1245Thr
ENST00000414678.6:c.2299G>A	ENSP00000412835.2:p.Ala767Thr
NM_017519.2:c.3733G>A	NP_059989.2:p.Ala1245Thr
NM_020732.3:c.3772G>A	NP_065783.3:p.Ala1258Thr
XM_005267069.3:c.3892G>A	XP_005267126.2:p.Ala1298Thr
XM_011535984.1:c.2971G>A	XP_011534286.1:p.Ala991Thr
XM_011535985.1:c.2791G>A	XP_011534287.1:p.Ala931Thr
XM_011535986.1:c.2551G>A	XP_011534288.1:p.Ala851Thr
XM_011535987.1:c.2170G>A	XP_011534289.1:p.Ala724Thr
XM_011535988.1:c.1033G>A	XP_011534290.1:p.Ala345Thr
NM_001346813.1:c.3892G>A	NP_001333742.1:p.Ala1298Thr
NM_001363725.1:c.1642G>A	NP_001350654.1:p.Ala548Thr
XM_011535984.2:c.4102G>A	XP_011534286.2:p.Ala1368Thr
XM_011535988.3:c.1033G>A	XP_011534290.1:p.Ala345Thr
XM_017011103.2:c.4003G>A	XP_016866592.1:p.Ala1335Thr
XM_017011104.1:c.3973G>A	XP_016866593.1:p.Ala1325Thr
XM_017011105.2:c.3943G>A	XP_016866594.1:p.Ala1315Thr
XM_017011106.2:c.3814G>A	XP_016866595.1:p.Ala1272Thr
XM_017011107.2:c.3793G>A	XP_016866596.1:p.Ala1265Thr
XR_002956289.1:n.4185G>A
NM_001363725.2:c.1642G>A	NP_001350654.1:p.Ala548Thr
NM_001371656.1:c.4021G>A	NP_001358585.1:p.Ala1341Thr
NM_001374820.1:c.4021G>A	NP_001361749.1:p.Ala1341Thr
NM_001374828.1:c.4141G>A MANE Select	NP_001361757.1:p.Ala1381Thr
NM_017519.3:c.3982G>A	NP_059989.3:p.Ala1328Thr