Canonical Allele Identifier: CA366242826

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522512C>G (hg19) ; chr6:g.157201378C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201378C>G , CM000668.2:g.157201378C>G	GRCh38
NC_000006.11:g.157522512C>G , CM000668.1:g.157522512C>G	GRCh37
NC_000006.10:g.157564204C>G	NCBI36
NG_032093.1:g.428449C>G
NG_032093.2:g.428449C>G
NG_066624.1:g.430353C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4994C>G	ENSP00000055163.8:p.Pro1665Arg
ENST00000414678.8:c.5063C>G	ENSP00000412835.3:p.Pro1688Arg
ENST00000637015.2:c.5282C>G	ENSP00000489729.2:p.Pro1761Arg
ENST00000346085.10:c.5033C>G	ENSP00000344546.5:p.Pro1678Arg
ENST00000350026.10:c.4745C>G	ENSP00000055163.7:p.Pro1582Arg
ENST00000414678.7:c.3311C>G	ENSP00000412835.2:p.Pro1104Arg
ENST00000635849.1:c.2474C>G	ENSP00000490948.1:p.Pro825Arg
ENST00000635957.1:c.2105C>G	ENSP00000490385.1:p.Pro702Arg
ENST00000636227.1:n.3616C>G
ENST00000636254.1:n.1073C>G
ENST00000636930.2:c.5153C>G MANE Select	ENSP00000490491.2:p.Pro1718Arg
ENST00000636940.1:n.3150C>G
ENST00000637015.1:c.2521C>G
ENST00000637568.1:c.2435C>G
ENST00000637741.1:n.1819C>G
ENST00000637810.1:c.2495C>G	ENSP00000489636.1:p.Pro832Arg
ENST00000637904.1:c.2654C>G	ENSP00000490550.1:p.Pro885Arg
ENST00000647938.1:c.4784C>G	ENSP00000498155.1:p.Pro1595Arg
ENST00000346085.9:c.4784C>G	ENSP00000344546.4:p.Pro1595Arg
ENST00000350026.9:c.4745C>G	ENSP00000055163.7:p.Pro1582Arg
ENST00000414678.6:c.3311C>G	ENSP00000412835.2:p.Pro1104Arg
NM_017519.2:c.4745C>G	NP_059989.2:p.Pro1582Arg
NM_020732.3:c.4784C>G	NP_065783.3:p.Pro1595Arg
XM_005267069.3:c.4904C>G	XP_005267126.2:p.Pro1635Arg
XM_011535984.1:c.3983C>G	XP_011534286.1:p.Pro1328Arg
XM_011535985.1:c.3803C>G	XP_011534287.1:p.Pro1268Arg
XM_011535986.1:c.3563C>G	XP_011534288.1:p.Pro1188Arg
XM_011535987.1:c.3182C>G	XP_011534289.1:p.Pro1061Arg
XM_011535988.1:c.2045C>G	XP_011534290.1:p.Pro682Arg
NM_001346813.1:c.4904C>G	NP_001333742.1:p.Pro1635Arg
NM_001363725.1:c.2654C>G	NP_001350654.1:p.Pro885Arg
XM_011535984.2:c.5114C>G	XP_011534286.2:p.Pro1705Arg
XM_011535988.3:c.2045C>G	XP_011534290.1:p.Pro682Arg
XM_017011103.2:c.5015C>G	XP_016866592.1:p.Pro1672Arg
XM_017011104.1:c.4985C>G	XP_016866593.1:p.Pro1662Arg
XM_017011105.2:c.4955C>G	XP_016866594.1:p.Pro1652Arg
XM_017011106.2:c.4826C>G	XP_016866595.1:p.Pro1609Arg
XM_017011107.2:c.4805C>G	XP_016866596.1:p.Pro1602Arg
XR_002956289.1:n.5100C>G
NM_001363725.2:c.2654C>G	NP_001350654.1:p.Pro885Arg
NM_001371656.1:c.5033C>G	NP_001358585.1:p.Pro1678Arg
NM_001374820.1:c.5033C>G	NP_001361749.1:p.Pro1678Arg
NM_001374828.1:c.5153C>G MANE Select	NP_001361757.1:p.Pro1718Arg
NM_017519.3:c.4994C>G	NP_059989.3:p.Pro1665Arg