Canonical Allele Identifier: CA366241344

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522107C>G (hg19) ; chr6:g.157200973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200973C>G , CM000668.2:g.157200973C>G	GRCh38
NC_000006.11:g.157522107C>G , CM000668.1:g.157522107C>G	GRCh37
NC_000006.10:g.157563799C>G	NCBI36
NG_032093.1:g.428044C>G
NG_032093.2:g.428044C>G
NG_066624.1:g.429948C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4589C>G	ENSP00000055163.8:p.Pro1530Arg
ENST00000414678.8:c.4658C>G	ENSP00000412835.3:p.Pro1553Arg
ENST00000637015.2:c.4877C>G	ENSP00000489729.2:p.Pro1626Arg
ENST00000346085.10:c.4628C>G	ENSP00000344546.5:p.Pro1543Arg
ENST00000350026.10:c.4340C>G	ENSP00000055163.7:p.Pro1447Arg
ENST00000414678.7:c.2906C>G	ENSP00000412835.2:p.Pro969Arg
ENST00000635849.1:c.2069C>G	ENSP00000490948.1:p.Pro690Arg
ENST00000635957.1:c.1700C>G	ENSP00000490385.1:p.Pro567Arg
ENST00000636227.1:n.3211C>G
ENST00000636254.1:n.668C>G
ENST00000636930.2:c.4748C>G MANE Select	ENSP00000490491.2:p.Pro1583Arg
ENST00000636940.1:n.2745C>G
ENST00000637015.1:c.2116C>G
ENST00000637568.1:c.2030C>G
ENST00000637741.1:n.1414C>G
ENST00000637810.1:c.2090C>G	ENSP00000489636.1:p.Pro697Arg
ENST00000637904.1:c.2249C>G	ENSP00000490550.1:p.Pro750Arg
ENST00000647938.1:c.4379C>G	ENSP00000498155.1:p.Pro1460Arg
ENST00000346085.9:c.4379C>G	ENSP00000344546.4:p.Pro1460Arg
ENST00000350026.9:c.4340C>G	ENSP00000055163.7:p.Pro1447Arg
ENST00000414678.6:c.2906C>G	ENSP00000412835.2:p.Pro969Arg
NM_017519.2:c.4340C>G	NP_059989.2:p.Pro1447Arg
NM_020732.3:c.4379C>G	NP_065783.3:p.Pro1460Arg
XM_005267069.3:c.4499C>G	XP_005267126.2:p.Pro1500Arg
XM_011535984.1:c.3578C>G	XP_011534286.1:p.Pro1193Arg
XM_011535985.1:c.3398C>G	XP_011534287.1:p.Pro1133Arg
XM_011535986.1:c.3158C>G	XP_011534288.1:p.Pro1053Arg
XM_011535987.1:c.2777C>G	XP_011534289.1:p.Pro926Arg
XM_011535988.1:c.1640C>G	XP_011534290.1:p.Pro547Arg
NM_001346813.1:c.4499C>G	NP_001333742.1:p.Pro1500Arg
NM_001363725.1:c.2249C>G	NP_001350654.1:p.Pro750Arg
XM_011535984.2:c.4709C>G	XP_011534286.2:p.Pro1570Arg
XM_011535988.3:c.1640C>G	XP_011534290.1:p.Pro547Arg
XM_017011103.2:c.4610C>G	XP_016866592.1:p.Pro1537Arg
XM_017011104.1:c.4580C>G	XP_016866593.1:p.Pro1527Arg
XM_017011105.2:c.4550C>G	XP_016866594.1:p.Pro1517Arg
XM_017011106.2:c.4421C>G	XP_016866595.1:p.Pro1474Arg
XM_017011107.2:c.4400C>G	XP_016866596.1:p.Pro1467Arg
XR_002956289.1:n.4695C>G
NM_001363725.2:c.2249C>G	NP_001350654.1:p.Pro750Arg
NM_001371656.1:c.4628C>G	NP_001358585.1:p.Pro1543Arg
NM_001374820.1:c.4628C>G	NP_001361749.1:p.Pro1543Arg
NM_001374828.1:c.4748C>G MANE Select	NP_001361757.1:p.Pro1583Arg
NM_017519.3:c.4589C>G	NP_059989.3:p.Pro1530Arg