Canonical Allele Identifier: CA366242883

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522524C>G (hg19) ; chr6:g.157201390C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201390C>G , CM000668.2:g.157201390C>G	GRCh38
NC_000006.11:g.157522524C>G , CM000668.1:g.157522524C>G	GRCh37
NC_000006.10:g.157564216C>G	NCBI36
NG_032093.1:g.428461C>G
NG_032093.2:g.428461C>G
NG_066624.1:g.430365C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5006C>G	ENSP00000055163.8:p.Pro1669Arg
ENST00000414678.8:c.5075C>G	ENSP00000412835.3:p.Pro1692Arg
ENST00000637015.2:c.5294C>G	ENSP00000489729.2:p.Pro1765Arg
ENST00000346085.10:c.5045C>G	ENSP00000344546.5:p.Pro1682Arg
ENST00000350026.10:c.4757C>G	ENSP00000055163.7:p.Pro1586Arg
ENST00000414678.7:c.3323C>G	ENSP00000412835.2:p.Pro1108Arg
ENST00000635849.1:c.2486C>G	ENSP00000490948.1:p.Pro829Arg
ENST00000635957.1:c.2117C>G	ENSP00000490385.1:p.Pro706Arg
ENST00000636227.1:n.3628C>G
ENST00000636254.1:n.1085C>G
ENST00000636930.2:c.5165C>G MANE Select	ENSP00000490491.2:p.Pro1722Arg
ENST00000636940.1:n.3162C>G
ENST00000637015.1:c.2533C>G
ENST00000637568.1:c.2447C>G
ENST00000637741.1:n.1831C>G
ENST00000637810.1:c.2507C>G	ENSP00000489636.1:p.Pro836Arg
ENST00000637904.1:c.2666C>G	ENSP00000490550.1:p.Pro889Arg
ENST00000647938.1:c.4796C>G	ENSP00000498155.1:p.Pro1599Arg
ENST00000346085.9:c.4796C>G	ENSP00000344546.4:p.Pro1599Arg
ENST00000350026.9:c.4757C>G	ENSP00000055163.7:p.Pro1586Arg
ENST00000414678.6:c.3323C>G	ENSP00000412835.2:p.Pro1108Arg
NM_017519.2:c.4757C>G	NP_059989.2:p.Pro1586Arg
NM_020732.3:c.4796C>G	NP_065783.3:p.Pro1599Arg
XM_005267069.3:c.4916C>G	XP_005267126.2:p.Pro1639Arg
XM_011535984.1:c.3995C>G	XP_011534286.1:p.Pro1332Arg
XM_011535985.1:c.3815C>G	XP_011534287.1:p.Pro1272Arg
XM_011535986.1:c.3575C>G	XP_011534288.1:p.Pro1192Arg
XM_011535987.1:c.3194C>G	XP_011534289.1:p.Pro1065Arg
XM_011535988.1:c.2057C>G	XP_011534290.1:p.Pro686Arg
NM_001346813.1:c.4916C>G	NP_001333742.1:p.Pro1639Arg
NM_001363725.1:c.2666C>G	NP_001350654.1:p.Pro889Arg
XM_011535984.2:c.5126C>G	XP_011534286.2:p.Pro1709Arg
XM_011535988.3:c.2057C>G	XP_011534290.1:p.Pro686Arg
XM_017011103.2:c.5027C>G	XP_016866592.1:p.Pro1676Arg
XM_017011104.1:c.4997C>G	XP_016866593.1:p.Pro1666Arg
XM_017011105.2:c.4967C>G	XP_016866594.1:p.Pro1656Arg
XM_017011106.2:c.4838C>G	XP_016866595.1:p.Pro1613Arg
XM_017011107.2:c.4817C>G	XP_016866596.1:p.Pro1606Arg
XR_002956289.1:n.5112C>G
NM_001363725.2:c.2666C>G	NP_001350654.1:p.Pro889Arg
NM_001371656.1:c.5045C>G	NP_001358585.1:p.Pro1682Arg
NM_001374820.1:c.5045C>G	NP_001361749.1:p.Pro1682Arg
NM_001374828.1:c.5165C>G MANE Select	NP_001361757.1:p.Pro1722Arg
NM_017519.3:c.5006C>G	NP_059989.3:p.Pro1669Arg