Canonical Allele Identifier: CA452978057

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522246A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201112A>C , CM000668.2:g.157201112A>C	GRCh38
NC_000006.11:g.157522246A>C , CM000668.1:g.157522246A>C	GRCh37
NC_000006.10:g.157563938A>C	NCBI36
NG_032093.1:g.428183A>C
NG_032093.2:g.428183A>C
NG_066624.1:g.430087A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4728A>C	ENSP00000055163.8:p.Ile1576=
ENST00000414678.8:c.4797A>C	ENSP00000412835.3:p.Ile1599=
ENST00000637015.2:c.5016A>C	ENSP00000489729.2:p.Ile1672=
ENST00000346085.10:c.4767A>C	ENSP00000344546.5:p.Ile1589=
ENST00000350026.10:c.4479A>C	ENSP00000055163.7:p.Ile1493=
ENST00000414678.7:c.3045A>C	ENSP00000412835.2:p.Ile1015=
ENST00000635849.1:c.2208A>C	ENSP00000490948.1:p.Ile736=
ENST00000635957.1:c.1839A>C	ENSP00000490385.1:p.Ile613=
ENST00000636227.1:n.3350A>C
ENST00000636254.1:n.807A>C
ENST00000636930.2:c.4887A>C MANE Select	ENSP00000490491.2:p.Ile1629=
ENST00000636940.1:n.2884A>C
ENST00000637015.1:c.2255A>C
ENST00000637568.1:c.2169A>C
ENST00000637741.1:n.1553A>C
ENST00000637810.1:c.2229A>C	ENSP00000489636.1:p.Ile743=
ENST00000637904.1:c.2388A>C	ENSP00000490550.1:p.Ile796=
ENST00000647938.1:c.4518A>C	ENSP00000498155.1:p.Ile1506=
ENST00000346085.9:c.4518A>C	ENSP00000344546.4:p.Ile1506=
ENST00000350026.9:c.4479A>C	ENSP00000055163.7:p.Ile1493=
ENST00000414678.6:c.3045A>C	ENSP00000412835.2:p.Ile1015=
NM_017519.2:c.4479A>C	NP_059989.2:p.Ile1493=
NM_020732.3:c.4518A>C	NP_065783.3:p.Ile1506=
XM_005267069.3:c.4638A>C	XP_005267126.2:p.Ile1546=
XM_011535984.1:c.3717A>C	XP_011534286.1:p.Ile1239=
XM_011535985.1:c.3537A>C	XP_011534287.1:p.Ile1179=
XM_011535986.1:c.3297A>C	XP_011534288.1:p.Ile1099=
XM_011535987.1:c.2916A>C	XP_011534289.1:p.Ile972=
XM_011535988.1:c.1779A>C	XP_011534290.1:p.Ile593=
NM_001346813.1:c.4638A>C	NP_001333742.1:p.Ile1546=
NM_001363725.1:c.2388A>C	NP_001350654.1:p.Ile796=
XM_011535984.2:c.4848A>C	XP_011534286.2:p.Ile1616=
XM_011535988.3:c.1779A>C	XP_011534290.1:p.Ile593=
XM_017011103.2:c.4749A>C	XP_016866592.1:p.Ile1583=
XM_017011104.1:c.4719A>C	XP_016866593.1:p.Ile1573=
XM_017011105.2:c.4689A>C	XP_016866594.1:p.Ile1563=
XM_017011106.2:c.4560A>C	XP_016866595.1:p.Ile1520=
XM_017011107.2:c.4539A>C	XP_016866596.1:p.Ile1513=
XR_002956289.1:n.4834A>C
NM_001363725.2:c.2388A>C	NP_001350654.1:p.Ile796=
NM_001371656.1:c.4767A>C	NP_001358585.1:p.Ile1589=
NM_001374820.1:c.4767A>C	NP_001361749.1:p.Ile1589=
NM_001374828.1:c.4887A>C MANE Select	NP_001361757.1:p.Ile1629=
NM_017519.3:c.4728A>C	NP_059989.3:p.Ile1576=