Canonical Allele Identifier: CA1675517057

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148876T= , CM000668.2:g.157148876T=	GRCh38
NC_000006.11:g.157470010T= , CM000668.1:g.157470010T=	GRCh37
NC_000006.10:g.157511702T=	NCBI36
NG_032093.1:g.375947T=
NG_032093.2:g.375947T=
NG_066624.1:g.377851T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3014T=	ENSP00000055163.8:p.Met1005=
ENST00000414678.8:c.2924T=	ENSP00000412835.3:p.Met975=
ENST00000637015.2:c.3014T=	ENSP00000489729.2:p.Met1005=
ENST00000319584.11:c.1028T=	ENSP00000313006.7:p.Met343=
ENST00000346085.10:c.3053T=	ENSP00000344546.5:p.Met1018=
ENST00000350026.10:c.2765T=	ENSP00000055163.7:p.Met922=
ENST00000414678.7:c.1172T=	ENSP00000412835.2:p.Met391=
ENST00000452544.2:n.915T=
ENST00000635849.1:c.335T=	ENSP00000490948.1:p.Met112=
ENST00000636426.1:n.148T=
ENST00000636930.2:c.3014T= MANE Select	ENSP00000490491.2:p.Met1005=
ENST00000637015.1:c.253T=
ENST00000637568.1:c.57T=
ENST00000637810.1:c.515T=	ENSP00000489636.1:p.Met172=
ENST00000637904.1:c.515T=	ENSP00000490550.1:p.Met172=
ENST00000647938.1:c.2804T=	ENSP00000498155.1:p.Met935=
ENST00000674190.1:n.1763T=
ENST00000319584.10:c.1031T=	ENSP00000313006.6:p.Met344=
ENST00000346085.9:c.2804T=	ENSP00000344546.4:p.Met935=
ENST00000350026.9:c.2765T=	ENSP00000055163.7:p.Met922=
ENST00000414678.6:c.1172T=	ENSP00000412835.2:p.Met391=
ENST00000452544.1:n.861T=
ENST00000478761.3:c.87T=
NM_017519.2:c.2765T=	NP_059989.2:p.Met922=
NM_020732.3:c.2804T=	NP_065783.3:p.Met935=
XM_005267069.3:c.2765T=	XP_005267126.2:p.Met922=
XM_011535984.1:c.1715T=	XP_011534286.1:p.Met572=
XM_011535985.1:c.1535T=	XP_011534287.1:p.Met512=
XM_011535986.1:c.1295T=	XP_011534288.1:p.Met432=
XM_011535987.1:c.914T=	XP_011534289.1:p.Met305=
XM_011535988.1:c.-20+15669T=	XP_011534290.1:n.-20+15669T=
NM_001346813.1:c.2765T=	NP_001333742.1:p.Met922=
NM_001363725.1:c.515T=	NP_001350654.1:p.Met172=
XM_011535984.2:c.2846T=	XP_011534286.2:p.Met949=
XM_011535988.3:c.-20+15669T=	XP_011534290.1:n.-20+15669T=
XM_017011103.2:c.2846T=	XP_016866592.1:p.Met949=
XM_017011104.1:c.2846T=	XP_016866593.1:p.Met949=
XM_017011105.2:c.2846T=	XP_016866594.1:p.Met949=
XM_017011106.2:c.2846T=	XP_016866595.1:p.Met949=
XM_017011107.2:c.2666T=	XP_016866596.1:p.Met889=
XR_002956289.1:n.2929T=
NM_001363725.2:c.515T=	NP_001350654.1:p.Met172=
NM_001371656.1:c.3053T=	NP_001358585.1:p.Met1018=
NM_001374820.1:c.3053T=	NP_001361749.1:p.Met1018=
NM_001374828.1:c.3014T= MANE Select	NP_001361757.1:p.Met1005=
NM_017519.3:c.3014T=	NP_059989.3:p.Met1005=