Canonical Allele Identifier: CA1675516983

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148697T= , CM000668.2:g.157148697T=	GRCh38
NC_000006.11:g.157469831T= , CM000668.1:g.157469831T=	GRCh37
NC_000006.10:g.157511523T=	NCBI36
NG_032093.1:g.375768T=
NG_032093.2:g.375768T=
NG_066624.1:g.377672T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2835T=	ENSP00000055163.8:p.Gly945=
ENST00000414678.8:c.2745T=	ENSP00000412835.3:p.Gly915=
ENST00000637015.2:c.2835T=	ENSP00000489729.2:p.Gly945=
ENST00000319584.11:c.849T=	ENSP00000313006.7:p.Gly283=
ENST00000346085.10:c.2874T=	ENSP00000344546.5:p.Gly958=
ENST00000350026.10:c.2586T=	ENSP00000055163.7:p.Gly862=
ENST00000414678.7:c.993T=	ENSP00000412835.2:p.Gly331=
ENST00000452544.2:n.736T=
ENST00000635849.1:c.156T=	ENSP00000490948.1:p.Gly52=
ENST00000636930.2:c.2835T= MANE Select	ENSP00000490491.2:p.Gly945=
ENST00000637015.1:c.74T=
ENST00000637810.1:c.336T=	ENSP00000489636.1:p.Gly112=
ENST00000637904.1:c.336T=	ENSP00000490550.1:p.Gly112=
ENST00000647938.1:c.2625T=	ENSP00000498155.1:p.Gly875=
ENST00000674190.1:n.1584T=
ENST00000319584.10:c.852T=	ENSP00000313006.6:p.Gly284=
ENST00000346085.9:c.2625T=	ENSP00000344546.4:p.Gly875=
ENST00000350026.9:c.2586T=	ENSP00000055163.7:p.Gly862=
ENST00000414678.6:c.993T=	ENSP00000412835.2:p.Gly331=
ENST00000452544.1:n.682T=
NM_017519.2:c.2586T=	NP_059989.2:p.Gly862=
NM_020732.3:c.2625T=	NP_065783.3:p.Gly875=
XM_005267069.3:c.2586T=	XP_005267126.2:p.Gly862=
XM_011535984.1:c.1536T=	XP_011534286.1:p.Gly512=
XM_011535985.1:c.1356T=	XP_011534287.1:p.Gly452=
XM_011535986.1:c.1116T=	XP_011534288.1:p.Gly372=
XM_011535987.1:c.735T=	XP_011534289.1:p.Gly245=
XM_011535988.1:c.-20+15490T=	XP_011534290.1:n.-20+15490T=
NM_001346813.1:c.2586T=	NP_001333742.1:p.Gly862=
NM_001363725.1:c.336T=	NP_001350654.1:p.Gly112=
XM_011535984.2:c.2667T=	XP_011534286.2:p.Gly889=
XM_011535988.3:c.-20+15490T=	XP_011534290.1:n.-20+15490T=
XM_017011103.2:c.2667T=	XP_016866592.1:p.Gly889=
XM_017011104.1:c.2667T=	XP_016866593.1:p.Gly889=
XM_017011105.2:c.2667T=	XP_016866594.1:p.Gly889=
XM_017011106.2:c.2667T=	XP_016866595.1:p.Gly889=
XM_017011107.2:c.2487T=	XP_016866596.1:p.Gly829=
XR_002956289.1:n.2750T=
NM_001363725.2:c.336T=	NP_001350654.1:p.Gly112=
NM_001371656.1:c.2874T=	NP_001358585.1:p.Gly958=
NM_001374820.1:c.2874T=	NP_001361749.1:p.Gly958=
NM_001374828.1:c.2835T= MANE Select	NP_001361757.1:p.Gly945=
NM_017519.3:c.2835T=	NP_059989.3:p.Gly945=