Canonical Allele Identifier: CA366242352

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522394C>G (hg19) ; chr6:g.157201260C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201260C>G , CM000668.2:g.157201260C>G	GRCh38
NC_000006.11:g.157522394C>G , CM000668.1:g.157522394C>G	GRCh37
NC_000006.10:g.157564086C>G	NCBI36
NG_032093.1:g.428331C>G
NG_032093.2:g.428331C>G
NG_066624.1:g.430235C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4876C>G	ENSP00000055163.8:p.Pro1626Ala
ENST00000414678.8:c.4945C>G	ENSP00000412835.3:p.Pro1649Ala
ENST00000637015.2:c.5164C>G	ENSP00000489729.2:p.Pro1722Ala
ENST00000346085.10:c.4915C>G	ENSP00000344546.5:p.Pro1639Ala
ENST00000350026.10:c.4627C>G	ENSP00000055163.7:p.Pro1543Ala
ENST00000414678.7:c.3193C>G	ENSP00000412835.2:p.Pro1065Ala
ENST00000635849.1:c.2356C>G	ENSP00000490948.1:p.Pro786Ala
ENST00000635957.1:c.1987C>G	ENSP00000490385.1:p.Pro663Ala
ENST00000636227.1:n.3498C>G
ENST00000636254.1:n.955C>G
ENST00000636930.2:c.5035C>G MANE Select	ENSP00000490491.2:p.Pro1679Ala
ENST00000636940.1:n.3032C>G
ENST00000637015.1:c.2403C>G
ENST00000637568.1:c.2317C>G
ENST00000637741.1:n.1701C>G
ENST00000637810.1:c.2377C>G	ENSP00000489636.1:p.Pro793Ala
ENST00000637904.1:c.2536C>G	ENSP00000490550.1:p.Pro846Ala
ENST00000647938.1:c.4666C>G	ENSP00000498155.1:p.Pro1556Ala
ENST00000346085.9:c.4666C>G	ENSP00000344546.4:p.Pro1556Ala
ENST00000350026.9:c.4627C>G	ENSP00000055163.7:p.Pro1543Ala
ENST00000414678.6:c.3193C>G	ENSP00000412835.2:p.Pro1065Ala
NM_017519.2:c.4627C>G	NP_059989.2:p.Pro1543Ala
NM_020732.3:c.4666C>G	NP_065783.3:p.Pro1556Ala
XM_005267069.3:c.4786C>G	XP_005267126.2:p.Pro1596Ala
XM_011535984.1:c.3865C>G	XP_011534286.1:p.Pro1289Ala
XM_011535985.1:c.3685C>G	XP_011534287.1:p.Pro1229Ala
XM_011535986.1:c.3445C>G	XP_011534288.1:p.Pro1149Ala
XM_011535987.1:c.3064C>G	XP_011534289.1:p.Pro1022Ala
XM_011535988.1:c.1927C>G	XP_011534290.1:p.Pro643Ala
NM_001346813.1:c.4786C>G	NP_001333742.1:p.Pro1596Ala
NM_001363725.1:c.2536C>G	NP_001350654.1:p.Pro846Ala
XM_011535984.2:c.4996C>G	XP_011534286.2:p.Pro1666Ala
XM_011535988.3:c.1927C>G	XP_011534290.1:p.Pro643Ala
XM_017011103.2:c.4897C>G	XP_016866592.1:p.Pro1633Ala
XM_017011104.1:c.4867C>G	XP_016866593.1:p.Pro1623Ala
XM_017011105.2:c.4837C>G	XP_016866594.1:p.Pro1613Ala
XM_017011106.2:c.4708C>G	XP_016866595.1:p.Pro1570Ala
XM_017011107.2:c.4687C>G	XP_016866596.1:p.Pro1563Ala
XR_002956289.1:n.4982C>G
NM_001363725.2:c.2536C>G	NP_001350654.1:p.Pro846Ala
NM_001371656.1:c.4915C>G	NP_001358585.1:p.Pro1639Ala
NM_001374820.1:c.4915C>G	NP_001361749.1:p.Pro1639Ala
NM_001374828.1:c.5035C>G MANE Select	NP_001361757.1:p.Pro1679Ala
NM_017519.3:c.4876C>G	NP_059989.3:p.Pro1626Ala