Canonical Allele Identifier: CA366238647

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196275C>T , CM000668.2:g.157196275C>T	GRCh38
NC_000006.11:g.157517409C>T , CM000668.1:g.157517409C>T	GRCh37
NC_000006.10:g.157559101C>T	NCBI36
NG_032093.1:g.423346C>T
NG_032093.2:g.423346C>T
NG_066624.1:g.425250C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4342C>T MANE Select	NP_001361757.1:p.Gln1448Ter
ENST00000636930.2:c.4342C>T MANE Select	ENSP00000490491.2:p.Gln1448Ter
NM_001346813.1:c.4093C>T	NP_001333742.1:p.Gln1365Ter
NM_001363725.1:c.1843C>T	NP_001350654.1:p.Gln615Ter
NM_001363725.2:c.1843C>T	NP_001350654.1:p.Gln615Ter
NM_001371656.1:c.4222C>T	NP_001358585.1:p.Gln1408Ter
NM_001374820.1:c.4222C>T	NP_001361749.1:p.Gln1408Ter
NM_017519.2:c.3934C>T	NP_059989.2:p.Gln1312Ter
NM_017519.3:c.4183C>T	NP_059989.3:p.Gln1395Ter
NM_020732.3:c.3973C>T	NP_065783.3:p.Gln1325Ter
ENST00000346085.10:c.4222C>T	ENSP00000344546.5:p.Gln1408Ter
ENST00000346085.9:c.3973C>T	ENSP00000344546.4:p.Gln1325Ter
ENST00000350026.10:c.3934C>T	ENSP00000055163.7:p.Gln1312Ter
ENST00000350026.11:c.4183C>T	ENSP00000055163.8:p.Gln1395Ter
ENST00000350026.9:c.3934C>T	ENSP00000055163.7:p.Gln1312Ter
ENST00000414678.6:c.2500C>T	ENSP00000412835.2:p.Gln834Ter
ENST00000414678.7:c.2500C>T	ENSP00000412835.2:p.Gln834Ter
ENST00000414678.8:c.4252C>T	ENSP00000412835.3:p.Gln1418Ter
ENST00000635849.1:c.1663C>T	ENSP00000490948.1:p.Gln555Ter
ENST00000635957.1:c.1294C>T	ENSP00000490385.1:p.Gln432Ter
ENST00000636227.1:n.2805C>T
ENST00000636940.1:n.2339C>T
ENST00000637015.1:c.1710C>T
ENST00000637015.2:c.4471C>T	ENSP00000489729.2:p.Gln1491Ter
ENST00000637568.1:c.1624C>T
ENST00000637741.1:n.1008C>T
ENST00000637810.1:c.1684C>T	ENSP00000489636.1:p.Gln562Ter
ENST00000637904.1:c.1843C>T	ENSP00000490550.1:p.Gln615Ter
ENST00000647938.1:c.3973C>T	ENSP00000498155.1:p.Gln1325Ter
XM_005267069.3:c.4093C>T	XP_005267126.2:p.Gln1365Ter
XM_011535984.1:c.3172C>T	XP_011534286.1:p.Gln1058Ter
XM_011535984.2:c.4303C>T	XP_011534286.2:p.Gln1435Ter
XM_011535985.1:c.2992C>T	XP_011534287.1:p.Gln998Ter
XM_011535986.1:c.2752C>T	XP_011534288.1:p.Gln918Ter
XM_011535987.1:c.2371C>T	XP_011534289.1:p.Gln791Ter
XM_011535988.1:c.1234C>T	XP_011534290.1:p.Gln412Ter
XM_011535988.3:c.1234C>T	XP_011534290.1:p.Gln412Ter
XM_017011103.2:c.4204C>T	XP_016866592.1:p.Gln1402Ter
XM_017011104.1:c.4174C>T	XP_016866593.1:p.Gln1392Ter
XM_017011105.2:c.4144C>T	XP_016866594.1:p.Gln1382Ter
XM_017011106.2:c.4015C>T	XP_016866595.1:p.Gln1339Ter
XM_017011107.2:c.3994C>T	XP_016866596.1:p.Gln1332Ter
XR_002956289.1:n.4386C>T