Canonical Allele Identifier: CA366241478

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522143C>G (hg19) ; chr6:g.157201009C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201009C>G , CM000668.2:g.157201009C>G	GRCh38
NC_000006.11:g.157522143C>G , CM000668.1:g.157522143C>G	GRCh37
NC_000006.10:g.157563835C>G	NCBI36
NG_032093.1:g.428080C>G
NG_032093.2:g.428080C>G
NG_066624.1:g.429984C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4625C>G	ENSP00000055163.8:p.Pro1542Arg
ENST00000414678.8:c.4694C>G	ENSP00000412835.3:p.Pro1565Arg
ENST00000637015.2:c.4913C>G	ENSP00000489729.2:p.Pro1638Arg
ENST00000346085.10:c.4664C>G	ENSP00000344546.5:p.Pro1555Arg
ENST00000350026.10:c.4376C>G	ENSP00000055163.7:p.Pro1459Arg
ENST00000414678.7:c.2942C>G	ENSP00000412835.2:p.Pro981Arg
ENST00000635849.1:c.2105C>G	ENSP00000490948.1:p.Pro702Arg
ENST00000635957.1:c.1736C>G	ENSP00000490385.1:p.Pro579Arg
ENST00000636227.1:n.3247C>G
ENST00000636254.1:n.704C>G
ENST00000636930.2:c.4784C>G MANE Select	ENSP00000490491.2:p.Pro1595Arg
ENST00000636940.1:n.2781C>G
ENST00000637015.1:c.2152C>G
ENST00000637568.1:c.2066C>G
ENST00000637741.1:n.1450C>G
ENST00000637810.1:c.2126C>G	ENSP00000489636.1:p.Pro709Arg
ENST00000637904.1:c.2285C>G	ENSP00000490550.1:p.Pro762Arg
ENST00000647938.1:c.4415C>G	ENSP00000498155.1:p.Pro1472Arg
ENST00000346085.9:c.4415C>G	ENSP00000344546.4:p.Pro1472Arg
ENST00000350026.9:c.4376C>G	ENSP00000055163.7:p.Pro1459Arg
ENST00000414678.6:c.2942C>G	ENSP00000412835.2:p.Pro981Arg
NM_017519.2:c.4376C>G	NP_059989.2:p.Pro1459Arg
NM_020732.3:c.4415C>G	NP_065783.3:p.Pro1472Arg
XM_005267069.3:c.4535C>G	XP_005267126.2:p.Pro1512Arg
XM_011535984.1:c.3614C>G	XP_011534286.1:p.Pro1205Arg
XM_011535985.1:c.3434C>G	XP_011534287.1:p.Pro1145Arg
XM_011535986.1:c.3194C>G	XP_011534288.1:p.Pro1065Arg
XM_011535987.1:c.2813C>G	XP_011534289.1:p.Pro938Arg
XM_011535988.1:c.1676C>G	XP_011534290.1:p.Pro559Arg
NM_001346813.1:c.4535C>G	NP_001333742.1:p.Pro1512Arg
NM_001363725.1:c.2285C>G	NP_001350654.1:p.Pro762Arg
XM_011535984.2:c.4745C>G	XP_011534286.2:p.Pro1582Arg
XM_011535988.3:c.1676C>G	XP_011534290.1:p.Pro559Arg
XM_017011103.2:c.4646C>G	XP_016866592.1:p.Pro1549Arg
XM_017011104.1:c.4616C>G	XP_016866593.1:p.Pro1539Arg
XM_017011105.2:c.4586C>G	XP_016866594.1:p.Pro1529Arg
XM_017011106.2:c.4457C>G	XP_016866595.1:p.Pro1486Arg
XM_017011107.2:c.4436C>G	XP_016866596.1:p.Pro1479Arg
XR_002956289.1:n.4731C>G
NM_001363725.2:c.2285C>G	NP_001350654.1:p.Pro762Arg
NM_001371656.1:c.4664C>G	NP_001358585.1:p.Pro1555Arg
NM_001374820.1:c.4664C>G	NP_001361749.1:p.Pro1555Arg
NM_001374828.1:c.4784C>G MANE Select	NP_001361757.1:p.Pro1595Arg
NM_017519.3:c.4625C>G	NP_059989.3:p.Pro1542Arg