Canonical Allele Identifier: CA452978301

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522435A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201301A>C , CM000668.2:g.157201301A>C	GRCh38
NC_000006.11:g.157522435A>C , CM000668.1:g.157522435A>C	GRCh37
NC_000006.10:g.157564127A>C	NCBI36
NG_032093.1:g.428372A>C
NG_032093.2:g.428372A>C
NG_066624.1:g.430276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4917A>C	ENSP00000055163.8:p.Pro1639=
ENST00000414678.8:c.4986A>C	ENSP00000412835.3:p.Pro1662=
ENST00000637015.2:c.5205A>C	ENSP00000489729.2:p.Pro1735=
ENST00000346085.10:c.4956A>C	ENSP00000344546.5:p.Pro1652=
ENST00000350026.10:c.4668A>C	ENSP00000055163.7:p.Pro1556=
ENST00000414678.7:c.3234A>C	ENSP00000412835.2:p.Pro1078=
ENST00000635849.1:c.2397A>C	ENSP00000490948.1:p.Pro799=
ENST00000635957.1:c.2028A>C	ENSP00000490385.1:p.Pro676=
ENST00000636227.1:n.3539A>C
ENST00000636254.1:n.996A>C
ENST00000636930.2:c.5076A>C MANE Select	ENSP00000490491.2:p.Pro1692=
ENST00000636940.1:n.3073A>C
ENST00000637015.1:c.2444A>C
ENST00000637568.1:c.2358A>C
ENST00000637741.1:n.1742A>C
ENST00000637810.1:c.2418A>C	ENSP00000489636.1:p.Pro806=
ENST00000637904.1:c.2577A>C	ENSP00000490550.1:p.Pro859=
ENST00000647938.1:c.4707A>C	ENSP00000498155.1:p.Pro1569=
ENST00000346085.9:c.4707A>C	ENSP00000344546.4:p.Pro1569=
ENST00000350026.9:c.4668A>C	ENSP00000055163.7:p.Pro1556=
ENST00000414678.6:c.3234A>C	ENSP00000412835.2:p.Pro1078=
NM_017519.2:c.4668A>C	NP_059989.2:p.Pro1556=
NM_020732.3:c.4707A>C	NP_065783.3:p.Pro1569=
XM_005267069.3:c.4827A>C	XP_005267126.2:p.Pro1609=
XM_011535984.1:c.3906A>C	XP_011534286.1:p.Pro1302=
XM_011535985.1:c.3726A>C	XP_011534287.1:p.Pro1242=
XM_011535986.1:c.3486A>C	XP_011534288.1:p.Pro1162=
XM_011535987.1:c.3105A>C	XP_011534289.1:p.Pro1035=
XM_011535988.1:c.1968A>C	XP_011534290.1:p.Pro656=
NM_001346813.1:c.4827A>C	NP_001333742.1:p.Pro1609=
NM_001363725.1:c.2577A>C	NP_001350654.1:p.Pro859=
XM_011535984.2:c.5037A>C	XP_011534286.2:p.Pro1679=
XM_011535988.3:c.1968A>C	XP_011534290.1:p.Pro656=
XM_017011103.2:c.4938A>C	XP_016866592.1:p.Pro1646=
XM_017011104.1:c.4908A>C	XP_016866593.1:p.Pro1636=
XM_017011105.2:c.4878A>C	XP_016866594.1:p.Pro1626=
XM_017011106.2:c.4749A>C	XP_016866595.1:p.Pro1583=
XM_017011107.2:c.4728A>C	XP_016866596.1:p.Pro1576=
XR_002956289.1:n.5023A>C
NM_001363725.2:c.2577A>C	NP_001350654.1:p.Pro859=
NM_001371656.1:c.4956A>C	NP_001358585.1:p.Pro1652=
NM_001374820.1:c.4956A>C	NP_001361749.1:p.Pro1652=
NM_001374828.1:c.5076A>C MANE Select	NP_001361757.1:p.Pro1692=
NM_017519.3:c.4917A>C	NP_059989.3:p.Pro1639=