Canonical Allele Identifier: CA1675543318

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207547T= , CM000668.2:g.157207547T=	GRCh38
NC_000006.11:g.157528681T= , CM000668.1:g.157528681T=	GRCh37
NC_000006.10:g.157570373T=	NCBI36
NG_032093.1:g.434618T=
NG_032093.2:g.434618T=
NG_066624.1:g.436522T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6775T= MANE Select	NP_001361757.1:p.Ser2259=
ENST00000636930.2:c.6775T= MANE Select	ENSP00000490491.2:p.Ser2259=
NM_001346813.1:c.6526T=	NP_001333742.1:p.Ser2176=
NM_001363725.1:c.4276T=	NP_001350654.1:p.Ser1426=
NM_001363725.2:c.4276T=	NP_001350654.1:p.Ser1426=
NM_001371656.1:c.6655T=	NP_001358585.1:p.Ser2219=
NM_001374820.1:c.6655T=	NP_001361749.1:p.Ser2219=
NM_017519.2:c.6367T=	NP_059989.2:p.Ser2123=
NM_017519.3:c.6616T=	NP_059989.3:p.Ser2206=
NM_020732.3:c.6406T=	NP_065783.3:p.Ser2136=
ENST00000346085.10:c.6655T=	ENSP00000344546.5:p.Ser2219=
ENST00000346085.9:c.6406T=	ENSP00000344546.4:p.Ser2136=
ENST00000350026.10:c.6367T=	ENSP00000055163.7:p.Ser2123=
ENST00000350026.11:c.6616T=	ENSP00000055163.8:p.Ser2206=
ENST00000350026.9:c.6367T=	ENSP00000055163.7:p.Ser2123=
ENST00000414678.6:c.4933T=	ENSP00000412835.2:p.Ser1645=
ENST00000414678.7:c.4933T=	ENSP00000412835.2:p.Ser1645=
ENST00000414678.8:c.6685T=	ENSP00000412835.3:p.Ser2229=
ENST00000635849.1:c.4096T=	ENSP00000490948.1:p.Ser1366=
ENST00000635928.1:c.875+56T=	ENSP00000489717.1:n.875+56T=
ENST00000635957.1:c.3727T=	ENSP00000490385.1:p.Ser1243=
ENST00000636227.1:n.5238T=
ENST00000636254.1:n.2695T=
ENST00000636940.1:n.4772T=
ENST00000637015.1:c.4143T=
ENST00000637015.2:c.6904T=	ENSP00000489729.2:p.Ser2302=
ENST00000637568.1:c.4057T=
ENST00000637741.1:n.3441T=
ENST00000637810.1:c.4117T=	ENSP00000489636.1:p.Ser1373=
ENST00000637904.1:c.4276T=	ENSP00000490550.1:p.Ser1426=
ENST00000637933.1:n.3890T=
ENST00000647938.1:c.6406T=	ENSP00000498155.1:p.Ser2136=
XM_005267069.3:c.6526T=	XP_005267126.2:p.Ser2176=
XM_011535984.1:c.5605T=	XP_011534286.1:p.Ser1869=
XM_011535984.2:c.6736T=	XP_011534286.2:p.Ser2246=
XM_011535985.1:c.5425T=	XP_011534287.1:p.Ser1809=
XM_011535986.1:c.5185T=	XP_011534288.1:p.Ser1729=
XM_011535987.1:c.4804T=	XP_011534289.1:p.Ser1602=
XM_011535988.1:c.3667T=	XP_011534290.1:p.Ser1223=
XM_011535988.3:c.3667T=	XP_011534290.1:p.Ser1223=
XM_017011103.2:c.6637T=	XP_016866592.1:p.Ser2213=
XM_017011104.1:c.6607T=	XP_016866593.1:p.Ser2203=
XM_017011105.2:c.6577T=	XP_016866594.1:p.Ser2193=
XM_017011106.2:c.6448T=	XP_016866595.1:p.Ser2150=
XM_017011107.2:c.6427T=	XP_016866596.1:p.Ser2143=
XR_002956289.1:n.6722T=