Canonical Allele Identifier: CA366242827

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4994C>A	ENSP00000055163.8:p.Pro1665Gln
ENST00000414678.8:c.5063C>A	ENSP00000412835.3:p.Pro1688Gln
ENST00000637015.2:c.5282C>A	ENSP00000489729.2:p.Pro1761Gln
ENST00000346085.10:c.5033C>A	ENSP00000344546.5:p.Pro1678Gln
ENST00000350026.10:c.4745C>A	ENSP00000055163.7:p.Pro1582Gln
ENST00000414678.7:c.3311C>A	ENSP00000412835.2:p.Pro1104Gln
ENST00000635849.1:c.2474C>A	ENSP00000490948.1:p.Pro825Gln
ENST00000635957.1:c.2105C>A	ENSP00000490385.1:p.Pro702Gln
ENST00000636227.1:n.3616C>A
ENST00000636254.1:n.1073C>A
ENST00000636930.2:c.5153C>A MANE Select	ENSP00000490491.2:p.Pro1718Gln
ENST00000636940.1:n.3150C>A
ENST00000637015.1:c.2521C>A
ENST00000637568.1:c.2435C>A
ENST00000637741.1:n.1819C>A
ENST00000637810.1:c.2495C>A	ENSP00000489636.1:p.Pro832Gln
ENST00000637904.1:c.2654C>A	ENSP00000490550.1:p.Pro885Gln
ENST00000647938.1:c.4784C>A	ENSP00000498155.1:p.Pro1595Gln
ENST00000346085.9:c.4784C>A	ENSP00000344546.4:p.Pro1595Gln
ENST00000350026.9:c.4745C>A	ENSP00000055163.7:p.Pro1582Gln
ENST00000414678.6:c.3311C>A	ENSP00000412835.2:p.Pro1104Gln
NM_017519.2:c.4745C>A	NP_059989.2:p.Pro1582Gln
NM_020732.3:c.4784C>A	NP_065783.3:p.Pro1595Gln
XM_005267069.3:c.4904C>A	XP_005267126.2:p.Pro1635Gln
XM_011535984.1:c.3983C>A	XP_011534286.1:p.Pro1328Gln
XM_011535985.1:c.3803C>A	XP_011534287.1:p.Pro1268Gln
XM_011535986.1:c.3563C>A	XP_011534288.1:p.Pro1188Gln
XM_011535987.1:c.3182C>A	XP_011534289.1:p.Pro1061Gln
XM_011535988.1:c.2045C>A	XP_011534290.1:p.Pro682Gln
NM_001346813.1:c.4904C>A	NP_001333742.1:p.Pro1635Gln
NM_001363725.1:c.2654C>A	NP_001350654.1:p.Pro885Gln
XM_011535984.2:c.5114C>A	XP_011534286.2:p.Pro1705Gln
XM_011535988.3:c.2045C>A	XP_011534290.1:p.Pro682Gln
XM_017011103.2:c.5015C>A	XP_016866592.1:p.Pro1672Gln
XM_017011104.1:c.4985C>A	XP_016866593.1:p.Pro1662Gln
XM_017011105.2:c.4955C>A	XP_016866594.1:p.Pro1652Gln
XM_017011106.2:c.4826C>A	XP_016866595.1:p.Pro1609Gln
XM_017011107.2:c.4805C>A	XP_016866596.1:p.Pro1602Gln
XR_002956289.1:n.5100C>A
NM_001363725.2:c.2654C>A	NP_001350654.1:p.Pro885Gln
NM_001371656.1:c.5033C>A	NP_001358585.1:p.Pro1678Gln
NM_001374820.1:c.5033C>A	NP_001361749.1:p.Pro1678Gln
NM_001374828.1:c.5153C>A MANE Select	NP_001361757.1:p.Pro1718Gln
NM_017519.3:c.4994C>A	NP_059989.3:p.Pro1665Gln