Canonical Allele Identifier: CA1675517032

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148820G= , CM000668.2:g.157148820G=	GRCh38
NC_000006.11:g.157469954G= , CM000668.1:g.157469954G=	GRCh37
NC_000006.10:g.157511646G=	NCBI36
NG_032093.1:g.375891G=
NG_032093.2:g.375891G=
NG_066624.1:g.377795G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2958G=	ENSP00000055163.8:p.Met986=
ENST00000414678.8:c.2868G=	ENSP00000412835.3:p.Met956=
ENST00000637015.2:c.2958G=	ENSP00000489729.2:p.Met986=
ENST00000319584.11:c.972G=	ENSP00000313006.7:p.Met324=
ENST00000346085.10:c.2997G=	ENSP00000344546.5:p.Met999=
ENST00000350026.10:c.2709G=	ENSP00000055163.7:p.Met903=
ENST00000414678.7:c.1116G=	ENSP00000412835.2:p.Met372=
ENST00000452544.2:n.859G=
ENST00000635849.1:c.279G=	ENSP00000490948.1:p.Met93=
ENST00000636426.1:n.92G=
ENST00000636930.2:c.2958G= MANE Select	ENSP00000490491.2:p.Met986=
ENST00000637015.1:c.197G=
ENST00000637568.1:c.1G=
ENST00000637810.1:c.459G=	ENSP00000489636.1:p.Met153=
ENST00000637904.1:c.459G=	ENSP00000490550.1:p.Met153=
ENST00000647938.1:c.2748G=	ENSP00000498155.1:p.Met916=
ENST00000674190.1:n.1707G=
ENST00000319584.10:c.975G=	ENSP00000313006.6:p.Met325=
ENST00000346085.9:c.2748G=	ENSP00000344546.4:p.Met916=
ENST00000350026.9:c.2709G=	ENSP00000055163.7:p.Met903=
ENST00000414678.6:c.1116G=	ENSP00000412835.2:p.Met372=
ENST00000452544.1:n.805G=
ENST00000478761.3:c.31G=
NM_017519.2:c.2709G=	NP_059989.2:p.Met903=
NM_020732.3:c.2748G=	NP_065783.3:p.Met916=
XM_005267069.3:c.2709G=	XP_005267126.2:p.Met903=
XM_011535984.1:c.1659G=	XP_011534286.1:p.Met553=
XM_011535985.1:c.1479G=	XP_011534287.1:p.Met493=
XM_011535986.1:c.1239G=	XP_011534288.1:p.Met413=
XM_011535987.1:c.858G=	XP_011534289.1:p.Met286=
XM_011535988.1:c.-20+15613G=	XP_011534290.1:n.-20+15613G=
NM_001346813.1:c.2709G=	NP_001333742.1:p.Met903=
NM_001363725.1:c.459G=	NP_001350654.1:p.Met153=
XM_011535984.2:c.2790G=	XP_011534286.2:p.Met930=
XM_011535988.3:c.-20+15613G=	XP_011534290.1:n.-20+15613G=
XM_017011103.2:c.2790G=	XP_016866592.1:p.Met930=
XM_017011104.1:c.2790G=	XP_016866593.1:p.Met930=
XM_017011105.2:c.2790G=	XP_016866594.1:p.Met930=
XM_017011106.2:c.2790G=	XP_016866595.1:p.Met930=
XM_017011107.2:c.2610G=	XP_016866596.1:p.Met870=
XR_002956289.1:n.2873G=
NM_001363725.2:c.459G=	NP_001350654.1:p.Met153=
NM_001371656.1:c.2997G=	NP_001358585.1:p.Met999=
NM_001374820.1:c.2997G=	NP_001361749.1:p.Met999=
NM_001374828.1:c.2958G= MANE Select	NP_001361757.1:p.Met986=
NM_017519.3:c.2958G=	NP_059989.3:p.Met986=