Canonical Allele Identifier: CA452784845

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201400-C-A
• MyVariant Identifiers: chr6:g.157522534C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201400C>A , CM000668.2:g.157201400C>A	GRCh38
NC_000006.11:g.157522534C>A , CM000668.1:g.157522534C>A	GRCh37
NC_000006.10:g.157564226C>A	NCBI36
NG_032093.1:g.428471C>A
NG_032093.2:g.428471C>A
NG_066624.1:g.430375C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5016C>A	ENSP00000055163.8:p.Ile1672=
ENST00000414678.8:c.5085C>A	ENSP00000412835.3:p.Ile1695=
ENST00000637015.2:c.5304C>A	ENSP00000489729.2:p.Ile1768=
ENST00000346085.10:c.5055C>A	ENSP00000344546.5:p.Ile1685=
ENST00000350026.10:c.4767C>A	ENSP00000055163.7:p.Ile1589=
ENST00000414678.7:c.3333C>A	ENSP00000412835.2:p.Ile1111=
ENST00000635849.1:c.2496C>A	ENSP00000490948.1:p.Ile832=
ENST00000635957.1:c.2127C>A	ENSP00000490385.1:p.Ile709=
ENST00000636227.1:n.3638C>A
ENST00000636254.1:n.1095C>A
ENST00000636930.2:c.5175C>A MANE Select	ENSP00000490491.2:p.Ile1725=
ENST00000636940.1:n.3172C>A
ENST00000637015.1:c.2543C>A
ENST00000637568.1:c.2457C>A
ENST00000637741.1:n.1841C>A
ENST00000637810.1:c.2517C>A	ENSP00000489636.1:p.Ile839=
ENST00000637904.1:c.2676C>A	ENSP00000490550.1:p.Ile892=
ENST00000647938.1:c.4806C>A	ENSP00000498155.1:p.Ile1602=
ENST00000346085.9:c.4806C>A	ENSP00000344546.4:p.Ile1602=
ENST00000350026.9:c.4767C>A	ENSP00000055163.7:p.Ile1589=
ENST00000414678.6:c.3333C>A	ENSP00000412835.2:p.Ile1111=
NM_017519.2:c.4767C>A	NP_059989.2:p.Ile1589=
NM_020732.3:c.4806C>A	NP_065783.3:p.Ile1602=
XM_005267069.3:c.4926C>A	XP_005267126.2:p.Ile1642=
XM_011535984.1:c.4005C>A	XP_011534286.1:p.Ile1335=
XM_011535985.1:c.3825C>A	XP_011534287.1:p.Ile1275=
XM_011535986.1:c.3585C>A	XP_011534288.1:p.Ile1195=
XM_011535987.1:c.3204C>A	XP_011534289.1:p.Ile1068=
XM_011535988.1:c.2067C>A	XP_011534290.1:p.Ile689=
NM_001346813.1:c.4926C>A	NP_001333742.1:p.Ile1642=
NM_001363725.1:c.2676C>A	NP_001350654.1:p.Ile892=
XM_011535984.2:c.5136C>A	XP_011534286.2:p.Ile1712=
XM_011535988.3:c.2067C>A	XP_011534290.1:p.Ile689=
XM_017011103.2:c.5037C>A	XP_016866592.1:p.Ile1679=
XM_017011104.1:c.5007C>A	XP_016866593.1:p.Ile1669=
XM_017011105.2:c.4977C>A	XP_016866594.1:p.Ile1659=
XM_017011106.2:c.4848C>A	XP_016866595.1:p.Ile1616=
XM_017011107.2:c.4827C>A	XP_016866596.1:p.Ile1609=
XR_002956289.1:n.5122C>A
NM_001363725.2:c.2676C>A	NP_001350654.1:p.Ile892=
NM_001371656.1:c.5055C>A	NP_001358585.1:p.Ile1685=
NM_001374820.1:c.5055C>A	NP_001361749.1:p.Ile1685=
NM_001374828.1:c.5175C>A MANE Select	NP_001361757.1:p.Ile1725=
NM_017519.3:c.5016C>A	NP_059989.3:p.Ile1672=