Canonical Allele Identifier: CA366242014

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374621
• MyVariant Identifiers: chr6:g.157522242G>A (hg19) ; chr6:g.157201108G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201108G>A , CM000668.2:g.157201108G>A	GRCh38
NC_000006.11:g.157522242G>A , CM000668.1:g.157522242G>A	GRCh37
NC_000006.10:g.157563934G>A	NCBI36
NG_032093.1:g.428179G>A
NG_032093.2:g.428179G>A
NG_066624.1:g.430083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4724G>A	ENSP00000055163.8:p.Arg1575Lys
ENST00000414678.8:c.4793G>A	ENSP00000412835.3:p.Arg1598Lys
ENST00000637015.2:c.5012G>A	ENSP00000489729.2:p.Arg1671Lys
ENST00000346085.10:c.4763G>A	ENSP00000344546.5:p.Arg1588Lys
ENST00000350026.10:c.4475G>A	ENSP00000055163.7:p.Arg1492Lys
ENST00000414678.7:c.3041G>A	ENSP00000412835.2:p.Arg1014Lys
ENST00000635849.1:c.2204G>A	ENSP00000490948.1:p.Arg735Lys
ENST00000635957.1:c.1835G>A	ENSP00000490385.1:p.Arg612Lys
ENST00000636227.1:n.3346G>A
ENST00000636254.1:n.803G>A
ENST00000636930.2:c.4883G>A MANE Select	ENSP00000490491.2:p.Arg1628Lys
ENST00000636940.1:n.2880G>A
ENST00000637015.1:c.2251G>A
ENST00000637568.1:c.2165G>A
ENST00000637741.1:n.1549G>A
ENST00000637810.1:c.2225G>A	ENSP00000489636.1:p.Arg742Lys
ENST00000637904.1:c.2384G>A	ENSP00000490550.1:p.Arg795Lys
ENST00000647938.1:c.4514G>A	ENSP00000498155.1:p.Arg1505Lys
ENST00000346085.9:c.4514G>A	ENSP00000344546.4:p.Arg1505Lys
ENST00000350026.9:c.4475G>A	ENSP00000055163.7:p.Arg1492Lys
ENST00000414678.6:c.3041G>A	ENSP00000412835.2:p.Arg1014Lys
NM_017519.2:c.4475G>A	NP_059989.2:p.Arg1492Lys
NM_020732.3:c.4514G>A	NP_065783.3:p.Arg1505Lys
XM_005267069.3:c.4634G>A	XP_005267126.2:p.Arg1545Lys
XM_011535984.1:c.3713G>A	XP_011534286.1:p.Arg1238Lys
XM_011535985.1:c.3533G>A	XP_011534287.1:p.Arg1178Lys
XM_011535986.1:c.3293G>A	XP_011534288.1:p.Arg1098Lys
XM_011535987.1:c.2912G>A	XP_011534289.1:p.Arg971Lys
XM_011535988.1:c.1775G>A	XP_011534290.1:p.Arg592Lys
NM_001346813.1:c.4634G>A	NP_001333742.1:p.Arg1545Lys
NM_001363725.1:c.2384G>A	NP_001350654.1:p.Arg795Lys
XM_011535984.2:c.4844G>A	XP_011534286.2:p.Arg1615Lys
XM_011535988.3:c.1775G>A	XP_011534290.1:p.Arg592Lys
XM_017011103.2:c.4745G>A	XP_016866592.1:p.Arg1582Lys
XM_017011104.1:c.4715G>A	XP_016866593.1:p.Arg1572Lys
XM_017011105.2:c.4685G>A	XP_016866594.1:p.Arg1562Lys
XM_017011106.2:c.4556G>A	XP_016866595.1:p.Arg1519Lys
XM_017011107.2:c.4535G>A	XP_016866596.1:p.Arg1512Lys
XR_002956289.1:n.4830G>A
NM_001363725.2:c.2384G>A	NP_001350654.1:p.Arg795Lys
NM_001371656.1:c.4763G>A	NP_001358585.1:p.Arg1588Lys
NM_001374820.1:c.4763G>A	NP_001361749.1:p.Arg1588Lys
NM_001374828.1:c.4883G>A MANE Select	NP_001361757.1:p.Arg1628Lys
NM_017519.3:c.4724G>A	NP_059989.3:p.Arg1575Lys