Canonical Allele Identifier: CA1675522927

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201071A= , CM000668.2:g.157201071A=	GRCh38
NC_000006.11:g.157522205A= , CM000668.1:g.157522205A=	GRCh37
NC_000006.10:g.157563897A=	NCBI36
NG_032093.1:g.428142A=
NG_032093.2:g.428142A=
NG_066624.1:g.430046A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4687A=	ENSP00000055163.8:p.Met1563=
ENST00000414678.8:c.4756A=	ENSP00000412835.3:p.Met1586=
ENST00000637015.2:c.4975A=	ENSP00000489729.2:p.Met1659=
ENST00000346085.10:c.4726A=	ENSP00000344546.5:p.Met1576=
ENST00000350026.10:c.4438A=	ENSP00000055163.7:p.Met1480=
ENST00000414678.7:c.3004A=	ENSP00000412835.2:p.Met1002=
ENST00000635849.1:c.2167A=	ENSP00000490948.1:p.Met723=
ENST00000635957.1:c.1798A=	ENSP00000490385.1:p.Met600=
ENST00000636227.1:n.3309A=
ENST00000636254.1:n.766A=
ENST00000636930.2:c.4846A= MANE Select	ENSP00000490491.2:p.Met1616=
ENST00000636940.1:n.2843A=
ENST00000637015.1:c.2214A=
ENST00000637568.1:c.2128A=
ENST00000637741.1:n.1512A=
ENST00000637810.1:c.2188A=	ENSP00000489636.1:p.Met730=
ENST00000637904.1:c.2347A=	ENSP00000490550.1:p.Met783=
ENST00000647938.1:c.4477A=	ENSP00000498155.1:p.Met1493=
ENST00000346085.9:c.4477A=	ENSP00000344546.4:p.Met1493=
ENST00000350026.9:c.4438A=	ENSP00000055163.7:p.Met1480=
ENST00000414678.6:c.3004A=	ENSP00000412835.2:p.Met1002=
NM_017519.2:c.4438A=	NP_059989.2:p.Met1480=
NM_020732.3:c.4477A=	NP_065783.3:p.Met1493=
XM_005267069.3:c.4597A=	XP_005267126.2:p.Met1533=
XM_011535984.1:c.3676A=	XP_011534286.1:p.Met1226=
XM_011535985.1:c.3496A=	XP_011534287.1:p.Met1166=
XM_011535986.1:c.3256A=	XP_011534288.1:p.Met1086=
XM_011535987.1:c.2875A=	XP_011534289.1:p.Met959=
XM_011535988.1:c.1738A=	XP_011534290.1:p.Met580=
NM_001346813.1:c.4597A=	NP_001333742.1:p.Met1533=
NM_001363725.1:c.2347A=	NP_001350654.1:p.Met783=
XM_011535984.2:c.4807A=	XP_011534286.2:p.Met1603=
XM_011535988.3:c.1738A=	XP_011534290.1:p.Met580=
XM_017011103.2:c.4708A=	XP_016866592.1:p.Met1570=
XM_017011104.1:c.4678A=	XP_016866593.1:p.Met1560=
XM_017011105.2:c.4648A=	XP_016866594.1:p.Met1550=
XM_017011106.2:c.4519A=	XP_016866595.1:p.Met1507=
XM_017011107.2:c.4498A=	XP_016866596.1:p.Met1500=
XR_002956289.1:n.4793A=
NM_001363725.2:c.2347A=	NP_001350654.1:p.Met783=
NM_001371656.1:c.4726A=	NP_001358585.1:p.Met1576=
NM_001374820.1:c.4726A=	NP_001361749.1:p.Met1576=
NM_001374828.1:c.4846A= MANE Select	NP_001361757.1:p.Met1616=
NM_017519.3:c.4687A=	NP_059989.3:p.Met1563=