Canonical Allele Identifier: CA366242188

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201182C>T , CM000668.2:g.157201182C>T	GRCh38
NC_000006.11:g.157522316C>T , CM000668.1:g.157522316C>T	GRCh37
NC_000006.10:g.157564008C>T	NCBI36
NG_032093.1:g.428253C>T
NG_032093.2:g.428253C>T
NG_066624.1:g.430157C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4957C>T MANE Select	NP_001361757.1:p.Gln1653Ter
ENST00000636930.2:c.4957C>T MANE Select	ENSP00000490491.2:p.Gln1653Ter
NM_001346813.1:c.4708C>T	NP_001333742.1:p.Gln1570Ter
NM_001363725.1:c.2458C>T	NP_001350654.1:p.Gln820Ter
NM_001363725.2:c.2458C>T	NP_001350654.1:p.Gln820Ter
NM_001371656.1:c.4837C>T	NP_001358585.1:p.Gln1613Ter
NM_001374820.1:c.4837C>T	NP_001361749.1:p.Gln1613Ter
NM_017519.2:c.4549C>T	NP_059989.2:p.Gln1517Ter
NM_017519.3:c.4798C>T	NP_059989.3:p.Gln1600Ter
NM_020732.3:c.4588C>T	NP_065783.3:p.Gln1530Ter
ENST00000346085.10:c.4837C>T	ENSP00000344546.5:p.Gln1613Ter
ENST00000346085.9:c.4588C>T	ENSP00000344546.4:p.Gln1530Ter
ENST00000350026.10:c.4549C>T	ENSP00000055163.7:p.Gln1517Ter
ENST00000350026.11:c.4798C>T	ENSP00000055163.8:p.Gln1600Ter
ENST00000350026.9:c.4549C>T	ENSP00000055163.7:p.Gln1517Ter
ENST00000414678.6:c.3115C>T	ENSP00000412835.2:p.Gln1039Ter
ENST00000414678.7:c.3115C>T	ENSP00000412835.2:p.Gln1039Ter
ENST00000414678.8:c.4867C>T	ENSP00000412835.3:p.Gln1623Ter
ENST00000635849.1:c.2278C>T	ENSP00000490948.1:p.Gln760Ter
ENST00000635957.1:c.1909C>T	ENSP00000490385.1:p.Gln637Ter
ENST00000636227.1:n.3420C>T
ENST00000636254.1:n.877C>T
ENST00000636940.1:n.2954C>T
ENST00000637015.1:c.2325C>T
ENST00000637015.2:c.5086C>T	ENSP00000489729.2:p.Gln1696Ter
ENST00000637568.1:c.2239C>T
ENST00000637741.1:n.1623C>T
ENST00000637810.1:c.2299C>T	ENSP00000489636.1:p.Gln767Ter
ENST00000637904.1:c.2458C>T	ENSP00000490550.1:p.Gln820Ter
ENST00000647938.1:c.4588C>T	ENSP00000498155.1:p.Gln1530Ter
XM_005267069.3:c.4708C>T	XP_005267126.2:p.Gln1570Ter
XM_011535984.1:c.3787C>T	XP_011534286.1:p.Gln1263Ter
XM_011535984.2:c.4918C>T	XP_011534286.2:p.Gln1640Ter
XM_011535985.1:c.3607C>T	XP_011534287.1:p.Gln1203Ter
XM_011535986.1:c.3367C>T	XP_011534288.1:p.Gln1123Ter
XM_011535987.1:c.2986C>T	XP_011534289.1:p.Gln996Ter
XM_011535988.1:c.1849C>T	XP_011534290.1:p.Gln617Ter
XM_011535988.3:c.1849C>T	XP_011534290.1:p.Gln617Ter
XM_017011103.2:c.4819C>T	XP_016866592.1:p.Gln1607Ter
XM_017011104.1:c.4789C>T	XP_016866593.1:p.Gln1597Ter
XM_017011105.2:c.4759C>T	XP_016866594.1:p.Gln1587Ter
XM_017011106.2:c.4630C>T	XP_016866595.1:p.Gln1544Ter
XM_017011107.2:c.4609C>T	XP_016866596.1:p.Gln1537Ter
XR_002956289.1:n.4904C>T