Canonical Allele Identifier: CA452781590

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190053-T-C
• MyVariant Identifiers: chr6:g.157511187T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190053T>C , CM000668.2:g.157190053T>C	GRCh38
NC_000006.11:g.157511187T>C , CM000668.1:g.157511187T>C	GRCh37
NC_000006.10:g.157552879T>C	NCBI36
NG_032093.1:g.417124T>C
NG_032093.2:g.417124T>C
NG_066624.1:g.419028T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3915T>C	ENSP00000055163.8:p.Ser1305=
ENST00000414678.8:c.3984T>C	ENSP00000412835.3:p.Ser1328=
ENST00000637015.2:c.4203T>C	ENSP00000489729.2:p.Ser1401=
ENST00000346085.10:c.3954T>C	ENSP00000344546.5:p.Ser1318=
ENST00000350026.10:c.3666T>C	ENSP00000055163.7:p.Ser1222=
ENST00000414678.7:c.2232T>C	ENSP00000412835.2:p.Ser744=
ENST00000635849.1:c.1395T>C	ENSP00000490948.1:p.Ser465=
ENST00000635957.1:c.1026T>C	ENSP00000490385.1:p.Ser342=
ENST00000636930.2:c.4074T>C MANE Select	ENSP00000490491.2:p.Ser1358=
ENST00000636940.1:n.2071T>C
ENST00000637015.1:c.1442T>C
ENST00000637568.1:c.1356T>C
ENST00000637741.1:n.740T>C
ENST00000637810.1:c.1416T>C	ENSP00000489636.1:p.Ser472=
ENST00000637904.1:c.1575T>C	ENSP00000490550.1:p.Ser525=
ENST00000647938.1:c.3705T>C	ENSP00000498155.1:p.Ser1235=
ENST00000346085.9:c.3705T>C	ENSP00000344546.4:p.Ser1235=
ENST00000350026.9:c.3666T>C	ENSP00000055163.7:p.Ser1222=
ENST00000414678.6:c.2232T>C	ENSP00000412835.2:p.Ser744=
NM_017519.2:c.3666T>C	NP_059989.2:p.Ser1222=
NM_020732.3:c.3705T>C	NP_065783.3:p.Ser1235=
XM_005267069.3:c.3825T>C	XP_005267126.2:p.Ser1275=
XM_011535984.1:c.2904T>C	XP_011534286.1:p.Ser968=
XM_011535985.1:c.2724T>C	XP_011534287.1:p.Ser908=
XM_011535986.1:c.2484T>C	XP_011534288.1:p.Ser828=
XM_011535987.1:c.2103T>C	XP_011534289.1:p.Ser701=
XM_011535988.1:c.966T>C	XP_011534290.1:p.Ser322=
NM_001346813.1:c.3825T>C	NP_001333742.1:p.Ser1275=
NM_001363725.1:c.1575T>C	NP_001350654.1:p.Ser525=
XM_011535984.2:c.4035T>C	XP_011534286.2:p.Ser1345=
XM_011535988.3:c.966T>C	XP_011534290.1:p.Ser322=
XM_017011103.2:c.3936T>C	XP_016866592.1:p.Ser1312=
XM_017011104.1:c.3906T>C	XP_016866593.1:p.Ser1302=
XM_017011105.2:c.3876T>C	XP_016866594.1:p.Ser1292=
XM_017011106.2:c.3747T>C	XP_016866595.1:p.Ser1249=
XM_017011107.2:c.3726T>C	XP_016866596.1:p.Ser1242=
XR_002956289.1:n.4118T>C
NM_001363725.2:c.1575T>C	NP_001350654.1:p.Ser525=
NM_001371656.1:c.3954T>C	NP_001358585.1:p.Ser1318=
NM_001374820.1:c.3954T>C	NP_001361749.1:p.Ser1318=
NM_001374828.1:c.4074T>C MANE Select	NP_001361757.1:p.Ser1358=
NM_017519.3:c.3915T>C	NP_059989.3:p.Ser1305=