Canonical Allele Identifier: CA366242942

Gene: ARID1B

Linked Data

• dbSNP Id: rs971931551
• MyVariant Identifiers: chr6:g.157522536G>C (hg19) ; chr6:g.157201402G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201402G>C , CM000668.2:g.157201402G>C	GRCh38
NC_000006.11:g.157522536G>C , CM000668.1:g.157522536G>C	GRCh37
NC_000006.10:g.157564228G>C	NCBI36
NG_032093.1:g.428473G>C
NG_032093.2:g.428473G>C
NG_066624.1:g.430377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5018G>C	ENSP00000055163.8:p.Arg1673Thr
ENST00000414678.8:c.5087G>C	ENSP00000412835.3:p.Arg1696Thr
ENST00000637015.2:c.5306G>C	ENSP00000489729.2:p.Arg1769Thr
ENST00000346085.10:c.5057G>C	ENSP00000344546.5:p.Arg1686Thr
ENST00000350026.10:c.4769G>C	ENSP00000055163.7:p.Arg1590Thr
ENST00000414678.7:c.3335G>C	ENSP00000412835.2:p.Arg1112Thr
ENST00000635849.1:c.2498G>C	ENSP00000490948.1:p.Arg833Thr
ENST00000635957.1:c.2129G>C	ENSP00000490385.1:p.Arg710Thr
ENST00000636227.1:n.3640G>C
ENST00000636254.1:n.1097G>C
ENST00000636930.2:c.5177G>C MANE Select	ENSP00000490491.2:p.Arg1726Thr
ENST00000636940.1:n.3174G>C
ENST00000637015.1:c.2545G>C
ENST00000637568.1:c.2459G>C
ENST00000637741.1:n.1843G>C
ENST00000637810.1:c.2519G>C	ENSP00000489636.1:p.Arg840Thr
ENST00000637904.1:c.2678G>C	ENSP00000490550.1:p.Arg893Thr
ENST00000647938.1:c.4808G>C	ENSP00000498155.1:p.Arg1603Thr
ENST00000346085.9:c.4808G>C	ENSP00000344546.4:p.Arg1603Thr
ENST00000350026.9:c.4769G>C	ENSP00000055163.7:p.Arg1590Thr
ENST00000414678.6:c.3335G>C	ENSP00000412835.2:p.Arg1112Thr
NM_017519.2:c.4769G>C	NP_059989.2:p.Arg1590Thr
NM_020732.3:c.4808G>C	NP_065783.3:p.Arg1603Thr
XM_005267069.3:c.4928G>C	XP_005267126.2:p.Arg1643Thr
XM_011535984.1:c.4007G>C	XP_011534286.1:p.Arg1336Thr
XM_011535985.1:c.3827G>C	XP_011534287.1:p.Arg1276Thr
XM_011535986.1:c.3587G>C	XP_011534288.1:p.Arg1196Thr
XM_011535987.1:c.3206G>C	XP_011534289.1:p.Arg1069Thr
XM_011535988.1:c.2069G>C	XP_011534290.1:p.Arg690Thr
NM_001346813.1:c.4928G>C	NP_001333742.1:p.Arg1643Thr
NM_001363725.1:c.2678G>C	NP_001350654.1:p.Arg893Thr
XM_011535984.2:c.5138G>C	XP_011534286.2:p.Arg1713Thr
XM_011535988.3:c.2069G>C	XP_011534290.1:p.Arg690Thr
XM_017011103.2:c.5039G>C	XP_016866592.1:p.Arg1680Thr
XM_017011104.1:c.5009G>C	XP_016866593.1:p.Arg1670Thr
XM_017011105.2:c.4979G>C	XP_016866594.1:p.Arg1660Thr
XM_017011106.2:c.4850G>C	XP_016866595.1:p.Arg1617Thr
XM_017011107.2:c.4829G>C	XP_016866596.1:p.Arg1610Thr
XR_002956289.1:n.5124G>C
NM_001363725.2:c.2678G>C	NP_001350654.1:p.Arg893Thr
NM_001371656.1:c.5057G>C	NP_001358585.1:p.Arg1686Thr
NM_001374820.1:c.5057G>C	NP_001361749.1:p.Arg1686Thr
NM_001374828.1:c.5177G>C MANE Select	NP_001361757.1:p.Arg1726Thr
NM_017519.3:c.5018G>C	NP_059989.3:p.Arg1673Thr