Canonical Allele Identifier: CA205348

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206450C>T , CM000668.2:g.157206450C>T	GRCh38
NC_000006.11:g.157527584C>T , CM000668.1:g.157527584C>T	GRCh37
NC_000006.10:g.157569276C>T	NCBI36
NG_032093.1:g.433521C>T
NG_032093.2:g.433521C>T
NG_066624.1:g.435425C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5678C>T MANE Select	NP_001361757.1:p.Ala1893Val
ENST00000636930.2:c.5678C>T MANE Select	ENSP00000490491.2:p.Ala1893Val
NM_001346813.1:c.5429C>T	NP_001333742.1:p.Ala1810Val
NM_001363725.1:c.3179C>T	NP_001350654.1:p.Ala1060Val
NM_001363725.2:c.3179C>T	NP_001350654.1:p.Ala1060Val
NM_001371656.1:c.5558C>T	NP_001358585.1:p.Ala1853Val
NM_001374820.1:c.5558C>T	NP_001361749.1:p.Ala1853Val
NM_017519.2:c.5270C>T	NP_059989.2:p.Ala1757Val
NM_017519.3:c.5519C>T	NP_059989.3:p.Ala1840Val
NM_020732.3:c.5309C>T	NP_065783.3:p.Ala1770Val
ENST00000346085.10:c.5558C>T	ENSP00000344546.5:p.Ala1853Val
ENST00000346085.9:c.5309C>T	ENSP00000344546.4:p.Ala1770Val
ENST00000350026.10:c.5270C>T	ENSP00000055163.7:p.Ala1757Val
ENST00000350026.11:c.5519C>T	ENSP00000055163.8:p.Ala1840Val
ENST00000350026.9:c.5270C>T	ENSP00000055163.7:p.Ala1757Val
ENST00000414678.6:c.3836C>T	ENSP00000412835.2:p.Ala1279Val
ENST00000414678.7:c.3836C>T	ENSP00000412835.2:p.Ala1279Val
ENST00000414678.8:c.5588C>T	ENSP00000412835.3:p.Ala1863Val
ENST00000635849.1:c.2999C>T	ENSP00000490948.1:p.Ala1000Val
ENST00000635957.1:c.2630C>T	ENSP00000490385.1:p.Ala877Val
ENST00000636227.1:n.4141C>T
ENST00000636254.1:n.1598C>T
ENST00000636940.1:n.3675C>T
ENST00000637015.1:c.3046C>T
ENST00000637015.2:c.5807C>T	ENSP00000489729.2:p.Ala1936Val
ENST00000637568.1:c.2960C>T
ENST00000637741.1:n.2344C>T
ENST00000637810.1:c.3020C>T	ENSP00000489636.1:p.Ala1007Val
ENST00000637904.1:c.3179C>T	ENSP00000490550.1:p.Ala1060Val
ENST00000637933.1:n.2793C>T
ENST00000647938.1:c.5309C>T	ENSP00000498155.1:p.Ala1770Val
XM_005267069.3:c.5429C>T	XP_005267126.2:p.Ala1810Val
XM_011535984.1:c.4508C>T	XP_011534286.1:p.Ala1503Val
XM_011535984.2:c.5639C>T	XP_011534286.2:p.Ala1880Val
XM_011535985.1:c.4328C>T	XP_011534287.1:p.Ala1443Val
XM_011535986.1:c.4088C>T	XP_011534288.1:p.Ala1363Val
XM_011535987.1:c.3707C>T	XP_011534289.1:p.Ala1236Val
XM_011535988.1:c.2570C>T	XP_011534290.1:p.Ala857Val
XM_011535988.3:c.2570C>T	XP_011534290.1:p.Ala857Val
XM_017011103.2:c.5540C>T	XP_016866592.1:p.Ala1847Val
XM_017011104.1:c.5510C>T	XP_016866593.1:p.Ala1837Val
XM_017011105.2:c.5480C>T	XP_016866594.1:p.Ala1827Val
XM_017011106.2:c.5351C>T	XP_016866595.1:p.Ala1784Val
XM_017011107.2:c.5330C>T	XP_016866596.1:p.Ala1777Val
XR_002956289.1:n.5625C>T