Canonical Allele Identifier: CA366249646

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207824C>A , CM000668.2:g.157207824C>A	GRCh38
NC_000006.11:g.157528958C>A , CM000668.1:g.157528958C>A	GRCh37
NC_000006.10:g.157570650C>A	NCBI36
NG_032093.1:g.434895C>A
NG_032093.2:g.434895C>A
NG_066624.1:g.436799C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.7052C>A MANE Select	NP_001361757.1:p.Ser2351Ter
ENST00000636930.2:c.7052C>A MANE Select	ENSP00000490491.2:p.Ser2351Ter
NM_001346813.1:c.6803C>A	NP_001333742.1:p.Ser2268Ter
NM_001363725.1:c.4553C>A	NP_001350654.1:p.Ser1518Ter
NM_001363725.2:c.4553C>A	NP_001350654.1:p.Ser1518Ter
NM_001371656.1:c.6932C>A	NP_001358585.1:p.Ser2311Ter
NM_001374820.1:c.6932C>A	NP_001361749.1:p.Ser2311Ter
NM_017519.2:c.6644C>A	NP_059989.2:p.Ser2215Ter
NM_017519.3:c.6893C>A	NP_059989.3:p.Ser2298Ter
NM_020732.3:c.6683C>A	NP_065783.3:p.Ser2228Ter
ENST00000346085.10:c.6932C>A	ENSP00000344546.5:p.Ser2311Ter
ENST00000346085.9:c.6683C>A	ENSP00000344546.4:p.Ser2228Ter
ENST00000350026.10:c.6644C>A	ENSP00000055163.7:p.Ser2215Ter
ENST00000350026.11:c.6893C>A	ENSP00000055163.8:p.Ser2298Ter
ENST00000350026.9:c.6644C>A	ENSP00000055163.7:p.Ser2215Ter
ENST00000414678.6:c.5210C>A	ENSP00000412835.2:p.Ser1737Ter
ENST00000414678.7:c.5210C>A	ENSP00000412835.2:p.Ser1737Ter
ENST00000414678.8:c.6962C>A	ENSP00000412835.3:p.Ser2321Ter
ENST00000635849.1:c.4373C>A	ENSP00000490948.1:p.Ser1458Ter
ENST00000635928.1:c.875+333C>A	ENSP00000489717.1:n.875+333C>A
ENST00000635957.1:c.4004C>A	ENSP00000490385.1:p.Ser1335Ter
ENST00000636227.1:n.5515C>A
ENST00000636254.1:n.2972C>A
ENST00000636940.1:n.5049C>A
ENST00000637015.1:c.4420C>A
ENST00000637015.2:c.7181C>A	ENSP00000489729.2:p.Ser2394Ter
ENST00000637568.1:c.4334C>A
ENST00000637741.1:n.3718C>A
ENST00000637810.1:c.4394C>A	ENSP00000489636.1:p.Ser1465Ter
ENST00000637904.1:c.4553C>A	ENSP00000490550.1:p.Ser1518Ter
ENST00000637933.1:n.4167C>A
ENST00000647938.1:c.6683C>A	ENSP00000498155.1:p.Ser2228Ter
XM_005267069.3:c.6803C>A	XP_005267126.2:p.Ser2268Ter
XM_011535984.1:c.5882C>A	XP_011534286.1:p.Ser1961Ter
XM_011535984.2:c.7013C>A	XP_011534286.2:p.Ser2338Ter
XM_011535985.1:c.5702C>A	XP_011534287.1:p.Ser1901Ter
XM_011535986.1:c.5462C>A	XP_011534288.1:p.Ser1821Ter
XM_011535987.1:c.5081C>A	XP_011534289.1:p.Ser1694Ter
XM_011535988.1:c.3944C>A	XP_011534290.1:p.Ser1315Ter
XM_011535988.3:c.3944C>A	XP_011534290.1:p.Ser1315Ter
XM_017011103.2:c.6914C>A	XP_016866592.1:p.Ser2305Ter
XM_017011104.1:c.6884C>A	XP_016866593.1:p.Ser2295Ter
XM_017011105.2:c.6854C>A	XP_016866594.1:p.Ser2285Ter
XM_017011106.2:c.6725C>A	XP_016866595.1:p.Ser2242Ter
XM_017011107.2:c.6704C>A	XP_016866596.1:p.Ser2235Ter
XR_002956289.1:n.6999C>A