Canonical Allele Identifier: CA452978398

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522183A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201049A>C , CM000668.2:g.157201049A>C	GRCh38
NC_000006.11:g.157522183A>C , CM000668.1:g.157522183A>C	GRCh37
NC_000006.10:g.157563875A>C	NCBI36
NG_032093.1:g.428120A>C
NG_032093.2:g.428120A>C
NG_066624.1:g.430024A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4665A>C	ENSP00000055163.8:p.Thr1555=
ENST00000414678.8:c.4734A>C	ENSP00000412835.3:p.Thr1578=
ENST00000637015.2:c.4953A>C	ENSP00000489729.2:p.Thr1651=
ENST00000346085.10:c.4704A>C	ENSP00000344546.5:p.Thr1568=
ENST00000350026.10:c.4416A>C	ENSP00000055163.7:p.Thr1472=
ENST00000414678.7:c.2982A>C	ENSP00000412835.2:p.Thr994=
ENST00000635849.1:c.2145A>C	ENSP00000490948.1:p.Thr715=
ENST00000635957.1:c.1776A>C	ENSP00000490385.1:p.Thr592=
ENST00000636227.1:n.3287A>C
ENST00000636254.1:n.744A>C
ENST00000636930.2:c.4824A>C MANE Select	ENSP00000490491.2:p.Thr1608=
ENST00000636940.1:n.2821A>C
ENST00000637015.1:c.2192A>C
ENST00000637568.1:c.2106A>C
ENST00000637741.1:n.1490A>C
ENST00000637810.1:c.2166A>C	ENSP00000489636.1:p.Thr722=
ENST00000637904.1:c.2325A>C	ENSP00000490550.1:p.Thr775=
ENST00000647938.1:c.4455A>C	ENSP00000498155.1:p.Thr1485=
ENST00000346085.9:c.4455A>C	ENSP00000344546.4:p.Thr1485=
ENST00000350026.9:c.4416A>C	ENSP00000055163.7:p.Thr1472=
ENST00000414678.6:c.2982A>C	ENSP00000412835.2:p.Thr994=
NM_017519.2:c.4416A>C	NP_059989.2:p.Thr1472=
NM_020732.3:c.4455A>C	NP_065783.3:p.Thr1485=
XM_005267069.3:c.4575A>C	XP_005267126.2:p.Thr1525=
XM_011535984.1:c.3654A>C	XP_011534286.1:p.Thr1218=
XM_011535985.1:c.3474A>C	XP_011534287.1:p.Thr1158=
XM_011535986.1:c.3234A>C	XP_011534288.1:p.Thr1078=
XM_011535987.1:c.2853A>C	XP_011534289.1:p.Thr951=
XM_011535988.1:c.1716A>C	XP_011534290.1:p.Thr572=
NM_001346813.1:c.4575A>C	NP_001333742.1:p.Thr1525=
NM_001363725.1:c.2325A>C	NP_001350654.1:p.Thr775=
XM_011535984.2:c.4785A>C	XP_011534286.2:p.Thr1595=
XM_011535988.3:c.1716A>C	XP_011534290.1:p.Thr572=
XM_017011103.2:c.4686A>C	XP_016866592.1:p.Thr1562=
XM_017011104.1:c.4656A>C	XP_016866593.1:p.Thr1552=
XM_017011105.2:c.4626A>C	XP_016866594.1:p.Thr1542=
XM_017011106.2:c.4497A>C	XP_016866595.1:p.Thr1499=
XM_017011107.2:c.4476A>C	XP_016866596.1:p.Thr1492=
XR_002956289.1:n.4771A>C
NM_001363725.2:c.2325A>C	NP_001350654.1:p.Thr775=
NM_001371656.1:c.4704A>C	NP_001358585.1:p.Thr1568=
NM_001374820.1:c.4704A>C	NP_001361749.1:p.Thr1568=
NM_001374828.1:c.4824A>C MANE Select	NP_001361757.1:p.Thr1608=
NM_017519.3:c.4665A>C	NP_059989.3:p.Thr1555=