Canonical Allele Identifier: CA366241509

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522149C>G (hg19) ; chr6:g.157201015C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201015C>G , CM000668.2:g.157201015C>G	GRCh38
NC_000006.11:g.157522149C>G , CM000668.1:g.157522149C>G	GRCh37
NC_000006.10:g.157563841C>G	NCBI36
NG_032093.1:g.428086C>G
NG_032093.2:g.428086C>G
NG_066624.1:g.429990C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4631C>G	ENSP00000055163.8:p.Pro1544Arg
ENST00000414678.8:c.4700C>G	ENSP00000412835.3:p.Pro1567Arg
ENST00000637015.2:c.4919C>G	ENSP00000489729.2:p.Pro1640Arg
ENST00000346085.10:c.4670C>G	ENSP00000344546.5:p.Pro1557Arg
ENST00000350026.10:c.4382C>G	ENSP00000055163.7:p.Pro1461Arg
ENST00000414678.7:c.2948C>G	ENSP00000412835.2:p.Pro983Arg
ENST00000635849.1:c.2111C>G	ENSP00000490948.1:p.Pro704Arg
ENST00000635957.1:c.1742C>G	ENSP00000490385.1:p.Pro581Arg
ENST00000636227.1:n.3253C>G
ENST00000636254.1:n.710C>G
ENST00000636930.2:c.4790C>G MANE Select	ENSP00000490491.2:p.Pro1597Arg
ENST00000636940.1:n.2787C>G
ENST00000637015.1:c.2158C>G
ENST00000637568.1:c.2072C>G
ENST00000637741.1:n.1456C>G
ENST00000637810.1:c.2132C>G	ENSP00000489636.1:p.Pro711Arg
ENST00000637904.1:c.2291C>G	ENSP00000490550.1:p.Pro764Arg
ENST00000647938.1:c.4421C>G	ENSP00000498155.1:p.Pro1474Arg
ENST00000346085.9:c.4421C>G	ENSP00000344546.4:p.Pro1474Arg
ENST00000350026.9:c.4382C>G	ENSP00000055163.7:p.Pro1461Arg
ENST00000414678.6:c.2948C>G	ENSP00000412835.2:p.Pro983Arg
NM_017519.2:c.4382C>G	NP_059989.2:p.Pro1461Arg
NM_020732.3:c.4421C>G	NP_065783.3:p.Pro1474Arg
XM_005267069.3:c.4541C>G	XP_005267126.2:p.Pro1514Arg
XM_011535984.1:c.3620C>G	XP_011534286.1:p.Pro1207Arg
XM_011535985.1:c.3440C>G	XP_011534287.1:p.Pro1147Arg
XM_011535986.1:c.3200C>G	XP_011534288.1:p.Pro1067Arg
XM_011535987.1:c.2819C>G	XP_011534289.1:p.Pro940Arg
XM_011535988.1:c.1682C>G	XP_011534290.1:p.Pro561Arg
NM_001346813.1:c.4541C>G	NP_001333742.1:p.Pro1514Arg
NM_001363725.1:c.2291C>G	NP_001350654.1:p.Pro764Arg
XM_011535984.2:c.4751C>G	XP_011534286.2:p.Pro1584Arg
XM_011535988.3:c.1682C>G	XP_011534290.1:p.Pro561Arg
XM_017011103.2:c.4652C>G	XP_016866592.1:p.Pro1551Arg
XM_017011104.1:c.4622C>G	XP_016866593.1:p.Pro1541Arg
XM_017011105.2:c.4592C>G	XP_016866594.1:p.Pro1531Arg
XM_017011106.2:c.4463C>G	XP_016866595.1:p.Pro1488Arg
XM_017011107.2:c.4442C>G	XP_016866596.1:p.Pro1481Arg
XR_002956289.1:n.4737C>G
NM_001363725.2:c.2291C>G	NP_001350654.1:p.Pro764Arg
NM_001371656.1:c.4670C>G	NP_001358585.1:p.Pro1557Arg
NM_001374820.1:c.4670C>G	NP_001361749.1:p.Pro1557Arg
NM_001374828.1:c.4790C>G MANE Select	NP_001361757.1:p.Pro1597Arg
NM_017519.3:c.4631C>G	NP_059989.3:p.Pro1544Arg