Canonical Allele Identifier: CA366242730

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376215
• MyVariant Identifiers: chr6:g.157522493A>G (hg19) ; chr6:g.157201359A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201359A>G , CM000668.2:g.157201359A>G	GRCh38
NC_000006.11:g.157522493A>G , CM000668.1:g.157522493A>G	GRCh37
NC_000006.10:g.157564185A>G	NCBI36
NG_032093.1:g.428430A>G
NG_032093.2:g.428430A>G
NG_066624.1:g.430334A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4975A>G	ENSP00000055163.8:p.Thr1659Ala
ENST00000414678.8:c.5044A>G	ENSP00000412835.3:p.Thr1682Ala
ENST00000637015.2:c.5263A>G	ENSP00000489729.2:p.Thr1755Ala
ENST00000346085.10:c.5014A>G	ENSP00000344546.5:p.Thr1672Ala
ENST00000350026.10:c.4726A>G	ENSP00000055163.7:p.Thr1576Ala
ENST00000414678.7:c.3292A>G	ENSP00000412835.2:p.Thr1098Ala
ENST00000635849.1:c.2455A>G	ENSP00000490948.1:p.Thr819Ala
ENST00000635957.1:c.2086A>G	ENSP00000490385.1:p.Thr696Ala
ENST00000636227.1:n.3597A>G
ENST00000636254.1:n.1054A>G
ENST00000636930.2:c.5134A>G MANE Select	ENSP00000490491.2:p.Thr1712Ala
ENST00000636940.1:n.3131A>G
ENST00000637015.1:c.2502A>G
ENST00000637568.1:c.2416A>G
ENST00000637741.1:n.1800A>G
ENST00000637810.1:c.2476A>G	ENSP00000489636.1:p.Thr826Ala
ENST00000637904.1:c.2635A>G	ENSP00000490550.1:p.Thr879Ala
ENST00000647938.1:c.4765A>G	ENSP00000498155.1:p.Thr1589Ala
ENST00000346085.9:c.4765A>G	ENSP00000344546.4:p.Thr1589Ala
ENST00000350026.9:c.4726A>G	ENSP00000055163.7:p.Thr1576Ala
ENST00000414678.6:c.3292A>G	ENSP00000412835.2:p.Thr1098Ala
NM_017519.2:c.4726A>G	NP_059989.2:p.Thr1576Ala
NM_020732.3:c.4765A>G	NP_065783.3:p.Thr1589Ala
XM_005267069.3:c.4885A>G	XP_005267126.2:p.Thr1629Ala
XM_011535984.1:c.3964A>G	XP_011534286.1:p.Thr1322Ala
XM_011535985.1:c.3784A>G	XP_011534287.1:p.Thr1262Ala
XM_011535986.1:c.3544A>G	XP_011534288.1:p.Thr1182Ala
XM_011535987.1:c.3163A>G	XP_011534289.1:p.Thr1055Ala
XM_011535988.1:c.2026A>G	XP_011534290.1:p.Thr676Ala
NM_001346813.1:c.4885A>G	NP_001333742.1:p.Thr1629Ala
NM_001363725.1:c.2635A>G	NP_001350654.1:p.Thr879Ala
XM_011535984.2:c.5095A>G	XP_011534286.2:p.Thr1699Ala
XM_011535988.3:c.2026A>G	XP_011534290.1:p.Thr676Ala
XM_017011103.2:c.4996A>G	XP_016866592.1:p.Thr1666Ala
XM_017011104.1:c.4966A>G	XP_016866593.1:p.Thr1656Ala
XM_017011105.2:c.4936A>G	XP_016866594.1:p.Thr1646Ala
XM_017011106.2:c.4807A>G	XP_016866595.1:p.Thr1603Ala
XM_017011107.2:c.4786A>G	XP_016866596.1:p.Thr1596Ala
XR_002956289.1:n.5081A>G
NM_001363725.2:c.2635A>G	NP_001350654.1:p.Thr879Ala
NM_001371656.1:c.5014A>G	NP_001358585.1:p.Thr1672Ala
NM_001374820.1:c.5014A>G	NP_001361749.1:p.Thr1672Ala
NM_001374828.1:c.5134A>G MANE Select	NP_001361757.1:p.Thr1712Ala
NM_017519.3:c.4975A>G	NP_059989.3:p.Thr1659Ala