Canonical Allele Identifier: CA452780754

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502172A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181038A>C , CM000668.2:g.157181038A>C	GRCh38
NC_000006.11:g.157502172A>C , CM000668.1:g.157502172A>C	GRCh37
NC_000006.10:g.157543864A>C	NCBI36
NG_032093.1:g.408109A>C
NG_032093.2:g.408109A>C
NG_066624.1:g.410013A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3415A>C	ENSP00000055163.8:p.Arg1139=
ENST00000414678.8:c.3484A>C	ENSP00000412835.3:p.Arg1162=
ENST00000637015.2:c.3703A>C	ENSP00000489729.2:p.Arg1235=
ENST00000319584.11:c.1588A>C	ENSP00000313006.7:p.Arg530=
ENST00000346085.10:c.3454A>C	ENSP00000344546.5:p.Arg1152=
ENST00000350026.10:c.3166A>C	ENSP00000055163.7:p.Arg1056=
ENST00000414678.7:c.1732A>C	ENSP00000412835.2:p.Arg578=
ENST00000635849.1:c.895A>C	ENSP00000490948.1:p.Arg299=
ENST00000635957.1:c.529A>C	ENSP00000490385.1:p.Arg177=
ENST00000636930.2:c.3574A>C MANE Select	ENSP00000490491.2:p.Arg1192=
ENST00000636940.1:n.1571A>C
ENST00000637015.1:c.942A>C
ENST00000637568.1:c.856A>C
ENST00000637741.1:n.240A>C
ENST00000637810.1:c.916A>C	ENSP00000489636.1:p.Arg306=
ENST00000637904.1:c.1075A>C	ENSP00000490550.1:p.Arg359=
ENST00000647938.1:c.3205A>C	ENSP00000498155.1:p.Arg1069=
ENST00000319584.10:c.1591A>C	ENSP00000313006.6:p.Arg531=
ENST00000346085.9:c.3205A>C	ENSP00000344546.4:p.Arg1069=
ENST00000350026.9:c.3166A>C	ENSP00000055163.7:p.Arg1056=
ENST00000400790.3:c.367A>C	ENSP00000383596.3:p.Arg123=
ENST00000414678.6:c.1732A>C	ENSP00000412835.2:p.Arg578=
ENST00000478761.3:c.776A>C
NM_017519.2:c.3166A>C	NP_059989.2:p.Arg1056=
NM_020732.3:c.3205A>C	NP_065783.3:p.Arg1069=
XM_005267069.3:c.3325A>C	XP_005267126.2:p.Arg1109=
XM_011535984.1:c.2404A>C	XP_011534286.1:p.Arg802=
XM_011535985.1:c.2224A>C	XP_011534287.1:p.Arg742=
XM_011535986.1:c.1984A>C	XP_011534288.1:p.Arg662=
XM_011535987.1:c.1603A>C	XP_011534289.1:p.Arg535=
XM_011535988.1:c.466A>C	XP_011534290.1:p.Arg156=
NM_001346813.1:c.3325A>C	NP_001333742.1:p.Arg1109=
NM_001363725.1:c.1075A>C	NP_001350654.1:p.Arg359=
XM_011535984.2:c.3535A>C	XP_011534286.2:p.Arg1179=
XM_011535988.3:c.466A>C	XP_011534290.1:p.Arg156=
XM_017011103.2:c.3436A>C	XP_016866592.1:p.Arg1146=
XM_017011104.1:c.3406A>C	XP_016866593.1:p.Arg1136=
XM_017011105.2:c.3376A>C	XP_016866594.1:p.Arg1126=
XM_017011106.2:c.3247A>C	XP_016866595.1:p.Arg1083=
XM_017011107.2:c.3226A>C	XP_016866596.1:p.Arg1076=
XR_002956289.1:n.3618A>C
NM_001363725.2:c.1075A>C	NP_001350654.1:p.Arg359=
NM_001371656.1:c.3454A>C	NP_001358585.1:p.Arg1152=
NM_001374820.1:c.3454A>C	NP_001361749.1:p.Arg1152=
NM_001374828.1:c.3574A>C MANE Select	NP_001361757.1:p.Arg1192=
NM_017519.3:c.3415A>C	NP_059989.3:p.Arg1139=