Canonical Allele Identifier: CA366388555

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157133192C>T , CM000668.2:g.157133192C>T	GRCh38
NC_000006.11:g.157454326C>T , CM000668.1:g.157454326C>T	GRCh37
NC_000006.10:g.157496018C>T	NCBI36
NG_032093.1:g.360263C>T
NG_032093.2:g.360263C>T
NG_066624.1:g.362167C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.2746C>T MANE Select	NP_001361757.1:p.Gln916Ter
ENST00000636930.2:c.2746C>T MANE Select	ENSP00000490491.2:p.Gln916Ter
NM_001346813.1:c.2497C>T	NP_001333742.1:p.Gln833Ter
NM_001363725.1:c.247C>T	NP_001350654.1:p.Gln83Ter
NM_001363725.2:c.247C>T	NP_001350654.1:p.Gln83Ter
NM_001371656.1:c.2785C>T	NP_001358585.1:p.Gln929Ter
NM_001374820.1:c.2785C>T	NP_001361749.1:p.Gln929Ter
NM_017519.2:c.2497C>T	NP_059989.2:p.Gln833Ter
NM_017519.3:c.2746C>T	NP_059989.3:p.Gln916Ter
NM_020732.3:c.2536C>T	NP_065783.3:p.Gln846Ter
ENST00000319584.10:c.763C>T	ENSP00000313006.6:p.Gln255Ter
ENST00000319584.11:c.760C>T	ENSP00000313006.7:p.Gln254Ter
ENST00000346085.10:c.2785C>T	ENSP00000344546.5:p.Gln929Ter
ENST00000346085.9:c.2536C>T	ENSP00000344546.4:p.Gln846Ter
ENST00000350026.10:c.2497C>T	ENSP00000055163.7:p.Gln833Ter
ENST00000350026.11:c.2746C>T	ENSP00000055163.8:p.Gln916Ter
ENST00000350026.9:c.2497C>T	ENSP00000055163.7:p.Gln833Ter
ENST00000414678.6:c.904C>T	ENSP00000412835.2:p.Gln302Ter
ENST00000414678.7:c.904C>T	ENSP00000412835.2:p.Gln302Ter
ENST00000414678.8:c.2656C>T	ENSP00000412835.3:p.Gln886Ter
ENST00000452544.1:n.593C>T
ENST00000452544.2:n.647C>T
ENST00000635849.1:c.83-15432C>T	ENSP00000490948.1:n.83-15432C>T
ENST00000637003.1:c.247C>T	ENSP00000489666.1:p.Gln83Ter
ENST00000637015.2:c.2746C>T	ENSP00000489729.2:p.Gln916Ter
ENST00000637810.1:c.247C>T	ENSP00000489636.1:p.Gln83Ter
ENST00000637904.1:c.247C>T	ENSP00000490550.1:p.Gln83Ter
ENST00000647938.1:c.2536C>T	ENSP00000498155.1:p.Gln846Ter
ENST00000674190.1:n.1495C>T
XM_005267069.3:c.2497C>T	XP_005267126.2:p.Gln833Ter
XM_011535984.1:c.1447C>T	XP_011534286.1:p.Gln483Ter
XM_011535984.2:c.2578C>T	XP_011534286.2:p.Gln860Ter
XM_011535985.1:c.1283-15432C>T	XP_011534287.1:n.1283-15432C>T
XM_011535986.1:c.1027C>T	XP_011534288.1:p.Gln343Ter
XM_011535987.1:c.646C>T	XP_011534289.1:p.Gln216Ter
XM_011535988.1:c.-35C>T	XP_011534290.1:n.-35C>T
XM_011535988.3:c.-35C>T	XP_011534290.1:n.-35C>T
XM_017011103.2:c.2578C>T	XP_016866592.1:p.Gln860Ter
XM_017011104.1:c.2578C>T	XP_016866593.1:p.Gln860Ter
XM_017011105.2:c.2578C>T	XP_016866594.1:p.Gln860Ter
XM_017011106.2:c.2578C>T	XP_016866595.1:p.Gln860Ter
XM_017011107.2:c.2414-15432C>T	XP_016866596.1:n.2414-15432C>T
XR_002956289.1:n.2661C>T