Canonical Allele Identifier: CA366242341

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522389C>A (hg19) ; chr6:g.157201255C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201255C>A , CM000668.2:g.157201255C>A	GRCh38
NC_000006.11:g.157522389C>A , CM000668.1:g.157522389C>A	GRCh37
NC_000006.10:g.157564081C>A	NCBI36
NG_032093.1:g.428326C>A
NG_032093.2:g.428326C>A
NG_066624.1:g.430230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4871C>A	ENSP00000055163.8:p.Pro1624His
ENST00000414678.8:c.4940C>A	ENSP00000412835.3:p.Pro1647His
ENST00000637015.2:c.5159C>A	ENSP00000489729.2:p.Pro1720His
ENST00000346085.10:c.4910C>A	ENSP00000344546.5:p.Pro1637His
ENST00000350026.10:c.4622C>A	ENSP00000055163.7:p.Pro1541His
ENST00000414678.7:c.3188C>A	ENSP00000412835.2:p.Pro1063His
ENST00000635849.1:c.2351C>A	ENSP00000490948.1:p.Pro784His
ENST00000635957.1:c.1982C>A	ENSP00000490385.1:p.Pro661His
ENST00000636227.1:n.3493C>A
ENST00000636254.1:n.950C>A
ENST00000636930.2:c.5030C>A MANE Select	ENSP00000490491.2:p.Pro1677His
ENST00000636940.1:n.3027C>A
ENST00000637015.1:c.2398C>A
ENST00000637568.1:c.2312C>A
ENST00000637741.1:n.1696C>A
ENST00000637810.1:c.2372C>A	ENSP00000489636.1:p.Pro791His
ENST00000637904.1:c.2531C>A	ENSP00000490550.1:p.Pro844His
ENST00000647938.1:c.4661C>A	ENSP00000498155.1:p.Pro1554His
ENST00000346085.9:c.4661C>A	ENSP00000344546.4:p.Pro1554His
ENST00000350026.9:c.4622C>A	ENSP00000055163.7:p.Pro1541His
ENST00000414678.6:c.3188C>A	ENSP00000412835.2:p.Pro1063His
NM_017519.2:c.4622C>A	NP_059989.2:p.Pro1541His
NM_020732.3:c.4661C>A	NP_065783.3:p.Pro1554His
XM_005267069.3:c.4781C>A	XP_005267126.2:p.Pro1594His
XM_011535984.1:c.3860C>A	XP_011534286.1:p.Pro1287His
XM_011535985.1:c.3680C>A	XP_011534287.1:p.Pro1227His
XM_011535986.1:c.3440C>A	XP_011534288.1:p.Pro1147His
XM_011535987.1:c.3059C>A	XP_011534289.1:p.Pro1020His
XM_011535988.1:c.1922C>A	XP_011534290.1:p.Pro641His
NM_001346813.1:c.4781C>A	NP_001333742.1:p.Pro1594His
NM_001363725.1:c.2531C>A	NP_001350654.1:p.Pro844His
XM_011535984.2:c.4991C>A	XP_011534286.2:p.Pro1664His
XM_011535988.3:c.1922C>A	XP_011534290.1:p.Pro641His
XM_017011103.2:c.4892C>A	XP_016866592.1:p.Pro1631His
XM_017011104.1:c.4862C>A	XP_016866593.1:p.Pro1621His
XM_017011105.2:c.4832C>A	XP_016866594.1:p.Pro1611His
XM_017011106.2:c.4703C>A	XP_016866595.1:p.Pro1568His
XM_017011107.2:c.4682C>A	XP_016866596.1:p.Pro1561His
XR_002956289.1:n.4977C>A
NM_001363725.2:c.2531C>A	NP_001350654.1:p.Pro844His
NM_001371656.1:c.4910C>A	NP_001358585.1:p.Pro1637His
NM_001374820.1:c.4910C>A	NP_001361749.1:p.Pro1637His
NM_001374828.1:c.5030C>A MANE Select	NP_001361757.1:p.Pro1677His
NM_017519.3:c.4871C>A	NP_059989.3:p.Pro1624His