Canonical Allele Identifier: CA366234796

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511192A>C (hg19) ; chr6:g.157190058A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190058A>C , CM000668.2:g.157190058A>C	GRCh38
NC_000006.11:g.157511192A>C , CM000668.1:g.157511192A>C	GRCh37
NC_000006.10:g.157552884A>C	NCBI36
NG_032093.1:g.417129A>C
NG_032093.2:g.417129A>C
NG_066624.1:g.419033A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3920A>C	ENSP00000055163.8:p.His1307Pro
ENST00000414678.8:c.3989A>C	ENSP00000412835.3:p.His1330Pro
ENST00000637015.2:c.4208A>C	ENSP00000489729.2:p.His1403Pro
ENST00000346085.10:c.3959A>C	ENSP00000344546.5:p.His1320Pro
ENST00000350026.10:c.3671A>C	ENSP00000055163.7:p.His1224Pro
ENST00000414678.7:c.2237A>C	ENSP00000412835.2:p.His746Pro
ENST00000635849.1:c.1400A>C	ENSP00000490948.1:p.His467Pro
ENST00000635957.1:c.1031A>C	ENSP00000490385.1:p.His344Pro
ENST00000636930.2:c.4079A>C MANE Select	ENSP00000490491.2:p.His1360Pro
ENST00000636940.1:n.2076A>C
ENST00000637015.1:c.1447A>C
ENST00000637568.1:c.1361A>C
ENST00000637741.1:n.745A>C
ENST00000637810.1:c.1421A>C	ENSP00000489636.1:p.His474Pro
ENST00000637904.1:c.1580A>C	ENSP00000490550.1:p.His527Pro
ENST00000647938.1:c.3710A>C	ENSP00000498155.1:p.His1237Pro
ENST00000346085.9:c.3710A>C	ENSP00000344546.4:p.His1237Pro
ENST00000350026.9:c.3671A>C	ENSP00000055163.7:p.His1224Pro
ENST00000414678.6:c.2237A>C	ENSP00000412835.2:p.His746Pro
NM_017519.2:c.3671A>C	NP_059989.2:p.His1224Pro
NM_020732.3:c.3710A>C	NP_065783.3:p.His1237Pro
XM_005267069.3:c.3830A>C	XP_005267126.2:p.His1277Pro
XM_011535984.1:c.2909A>C	XP_011534286.1:p.His970Pro
XM_011535985.1:c.2729A>C	XP_011534287.1:p.His910Pro
XM_011535986.1:c.2489A>C	XP_011534288.1:p.His830Pro
XM_011535987.1:c.2108A>C	XP_011534289.1:p.His703Pro
XM_011535988.1:c.971A>C	XP_011534290.1:p.His324Pro
NM_001346813.1:c.3830A>C	NP_001333742.1:p.His1277Pro
NM_001363725.1:c.1580A>C	NP_001350654.1:p.His527Pro
XM_011535984.2:c.4040A>C	XP_011534286.2:p.His1347Pro
XM_011535988.3:c.971A>C	XP_011534290.1:p.His324Pro
XM_017011103.2:c.3941A>C	XP_016866592.1:p.His1314Pro
XM_017011104.1:c.3911A>C	XP_016866593.1:p.His1304Pro
XM_017011105.2:c.3881A>C	XP_016866594.1:p.His1294Pro
XM_017011106.2:c.3752A>C	XP_016866595.1:p.His1251Pro
XM_017011107.2:c.3731A>C	XP_016866596.1:p.His1244Pro
XR_002956289.1:n.4123A>C
NM_001363725.2:c.1580A>C	NP_001350654.1:p.His527Pro
NM_001371656.1:c.3959A>C	NP_001358585.1:p.His1320Pro
NM_001374820.1:c.3959A>C	NP_001361749.1:p.His1320Pro
NM_001374828.1:c.4079A>C MANE Select	NP_001361757.1:p.His1360Pro
NM_017519.3:c.3920A>C	NP_059989.3:p.His1307Pro