Canonical Allele Identifier: CA366234802

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190058-A-G
• MyVariant Identifiers: chr6:g.157511192A>G (hg19) ; chr6:g.157190058A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3920A>G	ENSP00000055163.8:p.His1307Arg
ENST00000414678.8:c.3989A>G	ENSP00000412835.3:p.His1330Arg
ENST00000637015.2:c.4208A>G	ENSP00000489729.2:p.His1403Arg
ENST00000346085.10:c.3959A>G	ENSP00000344546.5:p.His1320Arg
ENST00000350026.10:c.3671A>G	ENSP00000055163.7:p.His1224Arg
ENST00000414678.7:c.2237A>G	ENSP00000412835.2:p.His746Arg
ENST00000635849.1:c.1400A>G	ENSP00000490948.1:p.His467Arg
ENST00000635957.1:c.1031A>G	ENSP00000490385.1:p.His344Arg
ENST00000636930.2:c.4079A>G MANE Select	ENSP00000490491.2:p.His1360Arg
ENST00000636940.1:n.2076A>G
ENST00000637015.1:c.1447A>G
ENST00000637568.1:c.1361A>G
ENST00000637741.1:n.745A>G
ENST00000637810.1:c.1421A>G	ENSP00000489636.1:p.His474Arg
ENST00000637904.1:c.1580A>G	ENSP00000490550.1:p.His527Arg
ENST00000647938.1:c.3710A>G	ENSP00000498155.1:p.His1237Arg
ENST00000346085.9:c.3710A>G	ENSP00000344546.4:p.His1237Arg
ENST00000350026.9:c.3671A>G	ENSP00000055163.7:p.His1224Arg
ENST00000414678.6:c.2237A>G	ENSP00000412835.2:p.His746Arg
NM_017519.2:c.3671A>G	NP_059989.2:p.His1224Arg
NM_020732.3:c.3710A>G	NP_065783.3:p.His1237Arg
XM_005267069.3:c.3830A>G	XP_005267126.2:p.His1277Arg
XM_011535984.1:c.2909A>G	XP_011534286.1:p.His970Arg
XM_011535985.1:c.2729A>G	XP_011534287.1:p.His910Arg
XM_011535986.1:c.2489A>G	XP_011534288.1:p.His830Arg
XM_011535987.1:c.2108A>G	XP_011534289.1:p.His703Arg
XM_011535988.1:c.971A>G	XP_011534290.1:p.His324Arg
NM_001346813.1:c.3830A>G	NP_001333742.1:p.His1277Arg
NM_001363725.1:c.1580A>G	NP_001350654.1:p.His527Arg
XM_011535984.2:c.4040A>G	XP_011534286.2:p.His1347Arg
XM_011535988.3:c.971A>G	XP_011534290.1:p.His324Arg
XM_017011103.2:c.3941A>G	XP_016866592.1:p.His1314Arg
XM_017011104.1:c.3911A>G	XP_016866593.1:p.His1304Arg
XM_017011105.2:c.3881A>G	XP_016866594.1:p.His1294Arg
XM_017011106.2:c.3752A>G	XP_016866595.1:p.His1251Arg
XM_017011107.2:c.3731A>G	XP_016866596.1:p.His1244Arg
XR_002956289.1:n.4123A>G
NM_001363725.2:c.1580A>G	NP_001350654.1:p.His527Arg
NM_001371656.1:c.3959A>G	NP_001358585.1:p.His1320Arg
NM_001374820.1:c.3959A>G	NP_001361749.1:p.His1320Arg
NM_001374828.1:c.4079A>G MANE Select	NP_001361757.1:p.His1360Arg
NM_017519.3:c.3920A>G	NP_059989.3:p.His1307Arg