Canonical Allele Identifier: CA4067696

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1226363
• ClinVar RCV Id: RCV001615628
• dbSNP Id: rs61745210
• ExAC: 6:157522090 G / A
• gnomAD v2: 6-157522090-G-A
• gnomAD v3: 6-157200956-G-A
• gnomAD v4: 6-157200956-G-A
• MyVariant Identifiers: chr6:g.157522090G>A (hg19) ; chr6:g.157200956G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200956G>A , CM000668.2:g.157200956G>A	GRCh38
NC_000006.11:g.157522090G>A , CM000668.1:g.157522090G>A	GRCh37
NC_000006.10:g.157563782G>A	NCBI36
NG_032093.1:g.428027G>A
NG_032093.2:g.428027G>A
NG_066624.1:g.429931G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4572G>A	ENSP00000055163.8:p.Ser1524=
ENST00000414678.8:c.4641G>A	ENSP00000412835.3:p.Ser1547=
ENST00000637015.2:c.4860G>A	ENSP00000489729.2:p.Ser1620=
ENST00000346085.10:c.4611G>A	ENSP00000344546.5:p.Ser1537=
ENST00000350026.10:c.4323G>A	ENSP00000055163.7:p.Ser1441=
ENST00000414678.7:c.2889G>A	ENSP00000412835.2:p.Ser963=
ENST00000635849.1:c.2052G>A	ENSP00000490948.1:p.Ser684=
ENST00000635957.1:c.1683G>A	ENSP00000490385.1:p.Ser561=
ENST00000636227.1:n.3194G>A
ENST00000636254.1:n.651G>A
ENST00000636930.2:c.4731G>A MANE Select	ENSP00000490491.2:p.Ser1577=
ENST00000636940.1:n.2728G>A
ENST00000637015.1:c.2099G>A
ENST00000637568.1:c.2013G>A
ENST00000637741.1:n.1397G>A
ENST00000637810.1:c.2073G>A	ENSP00000489636.1:p.Ser691=
ENST00000637904.1:c.2232G>A	ENSP00000490550.1:p.Ser744=
ENST00000647938.1:c.4362G>A	ENSP00000498155.1:p.Ser1454=
ENST00000346085.9:c.4362G>A	ENSP00000344546.4:p.Ser1454=
ENST00000350026.9:c.4323G>A	ENSP00000055163.7:p.Ser1441=
ENST00000414678.6:c.2889G>A	ENSP00000412835.2:p.Ser963=
NM_017519.2:c.4323G>A	NP_059989.2:p.Ser1441=
NM_020732.3:c.4362G>A	NP_065783.3:p.Ser1454=
XM_005267069.3:c.4482G>A	XP_005267126.2:p.Ser1494=
XM_011535984.1:c.3561G>A	XP_011534286.1:p.Ser1187=
XM_011535985.1:c.3381G>A	XP_011534287.1:p.Ser1127=
XM_011535986.1:c.3141G>A	XP_011534288.1:p.Ser1047=
XM_011535987.1:c.2760G>A	XP_011534289.1:p.Ser920=
XM_011535988.1:c.1623G>A	XP_011534290.1:p.Ser541=
NM_001346813.1:c.4482G>A	NP_001333742.1:p.Ser1494=
NM_001363725.1:c.2232G>A	NP_001350654.1:p.Ser744=
XM_011535984.2:c.4692G>A	XP_011534286.2:p.Ser1564=
XM_011535988.3:c.1623G>A	XP_011534290.1:p.Ser541=
XM_017011103.2:c.4593G>A	XP_016866592.1:p.Ser1531=
XM_017011104.1:c.4563G>A	XP_016866593.1:p.Ser1521=
XM_017011105.2:c.4533G>A	XP_016866594.1:p.Ser1511=
XM_017011106.2:c.4404G>A	XP_016866595.1:p.Ser1468=
XM_017011107.2:c.4383G>A	XP_016866596.1:p.Ser1461=
XR_002956289.1:n.4678G>A
NM_001363725.2:c.2232G>A	NP_001350654.1:p.Ser744=
NM_001371656.1:c.4611G>A	NP_001358585.1:p.Ser1537=
NM_001374820.1:c.4611G>A	NP_001361749.1:p.Ser1537=
NM_001374828.1:c.4731G>A MANE Select	NP_001361757.1:p.Ser1577=
NM_017519.3:c.4572G>A	NP_059989.3:p.Ser1524=