Canonical Allele Identifier: CA366241247

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522062C>G (hg19) ; chr6:g.157200928C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200928C>G , CM000668.2:g.157200928C>G	GRCh38
NC_000006.11:g.157522062C>G , CM000668.1:g.157522062C>G	GRCh37
NC_000006.10:g.157563754C>G	NCBI36
NG_032093.1:g.427999C>G
NG_032093.2:g.427999C>G
NG_066624.1:g.429903C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4544C>G	ENSP00000055163.8:p.Pro1515Arg
ENST00000414678.8:c.4613C>G	ENSP00000412835.3:p.Pro1538Arg
ENST00000637015.2:c.4832C>G	ENSP00000489729.2:p.Pro1611Arg
ENST00000346085.10:c.4583C>G	ENSP00000344546.5:p.Pro1528Arg
ENST00000350026.10:c.4295C>G	ENSP00000055163.7:p.Pro1432Arg
ENST00000414678.7:c.2861C>G	ENSP00000412835.2:p.Pro954Arg
ENST00000635849.1:c.2024C>G	ENSP00000490948.1:p.Pro675Arg
ENST00000635957.1:c.1655C>G	ENSP00000490385.1:p.Pro552Arg
ENST00000636227.1:n.3166C>G
ENST00000636254.1:n.623C>G
ENST00000636930.2:c.4703C>G MANE Select	ENSP00000490491.2:p.Pro1568Arg
ENST00000636940.1:n.2700C>G
ENST00000637015.1:c.2071C>G
ENST00000637568.1:c.1985C>G
ENST00000637741.1:n.1369C>G
ENST00000637810.1:c.2045C>G	ENSP00000489636.1:p.Pro682Arg
ENST00000637904.1:c.2204C>G	ENSP00000490550.1:p.Pro735Arg
ENST00000647938.1:c.4334C>G	ENSP00000498155.1:p.Pro1445Arg
ENST00000346085.9:c.4334C>G	ENSP00000344546.4:p.Pro1445Arg
ENST00000350026.9:c.4295C>G	ENSP00000055163.7:p.Pro1432Arg
ENST00000414678.6:c.2861C>G	ENSP00000412835.2:p.Pro954Arg
NM_017519.2:c.4295C>G	NP_059989.2:p.Pro1432Arg
NM_020732.3:c.4334C>G	NP_065783.3:p.Pro1445Arg
XM_005267069.3:c.4454C>G	XP_005267126.2:p.Pro1485Arg
XM_011535984.1:c.3533C>G	XP_011534286.1:p.Pro1178Arg
XM_011535985.1:c.3353C>G	XP_011534287.1:p.Pro1118Arg
XM_011535986.1:c.3113C>G	XP_011534288.1:p.Pro1038Arg
XM_011535987.1:c.2732C>G	XP_011534289.1:p.Pro911Arg
XM_011535988.1:c.1595C>G	XP_011534290.1:p.Pro532Arg
NM_001346813.1:c.4454C>G	NP_001333742.1:p.Pro1485Arg
NM_001363725.1:c.2204C>G	NP_001350654.1:p.Pro735Arg
XM_011535984.2:c.4664C>G	XP_011534286.2:p.Pro1555Arg
XM_011535988.3:c.1595C>G	XP_011534290.1:p.Pro532Arg
XM_017011103.2:c.4565C>G	XP_016866592.1:p.Pro1522Arg
XM_017011104.1:c.4535C>G	XP_016866593.1:p.Pro1512Arg
XM_017011105.2:c.4505C>G	XP_016866594.1:p.Pro1502Arg
XM_017011106.2:c.4376C>G	XP_016866595.1:p.Pro1459Arg
XM_017011107.2:c.4355C>G	XP_016866596.1:p.Pro1452Arg
XR_002956289.1:n.4650C>G
NM_001363725.2:c.2204C>G	NP_001350654.1:p.Pro735Arg
NM_001371656.1:c.4583C>G	NP_001358585.1:p.Pro1528Arg
NM_001374820.1:c.4583C>G	NP_001361749.1:p.Pro1528Arg
NM_001374828.1:c.4703C>G MANE Select	NP_001361757.1:p.Pro1568Arg
NM_017519.3:c.4544C>G	NP_059989.3:p.Pro1515Arg