Canonical Allele Identifier: CA366242015

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522242G>C (hg19) ; chr6:g.157201108G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4724G>C	ENSP00000055163.8:p.Arg1575Thr
ENST00000414678.8:c.4793G>C	ENSP00000412835.3:p.Arg1598Thr
ENST00000637015.2:c.5012G>C	ENSP00000489729.2:p.Arg1671Thr
ENST00000346085.10:c.4763G>C	ENSP00000344546.5:p.Arg1588Thr
ENST00000350026.10:c.4475G>C	ENSP00000055163.7:p.Arg1492Thr
ENST00000414678.7:c.3041G>C	ENSP00000412835.2:p.Arg1014Thr
ENST00000635849.1:c.2204G>C	ENSP00000490948.1:p.Arg735Thr
ENST00000635957.1:c.1835G>C	ENSP00000490385.1:p.Arg612Thr
ENST00000636227.1:n.3346G>C
ENST00000636254.1:n.803G>C
ENST00000636930.2:c.4883G>C MANE Select	ENSP00000490491.2:p.Arg1628Thr
ENST00000636940.1:n.2880G>C
ENST00000637015.1:c.2251G>C
ENST00000637568.1:c.2165G>C
ENST00000637741.1:n.1549G>C
ENST00000637810.1:c.2225G>C	ENSP00000489636.1:p.Arg742Thr
ENST00000637904.1:c.2384G>C	ENSP00000490550.1:p.Arg795Thr
ENST00000647938.1:c.4514G>C	ENSP00000498155.1:p.Arg1505Thr
ENST00000346085.9:c.4514G>C	ENSP00000344546.4:p.Arg1505Thr
ENST00000350026.9:c.4475G>C	ENSP00000055163.7:p.Arg1492Thr
ENST00000414678.6:c.3041G>C	ENSP00000412835.2:p.Arg1014Thr
NM_017519.2:c.4475G>C	NP_059989.2:p.Arg1492Thr
NM_020732.3:c.4514G>C	NP_065783.3:p.Arg1505Thr
XM_005267069.3:c.4634G>C	XP_005267126.2:p.Arg1545Thr
XM_011535984.1:c.3713G>C	XP_011534286.1:p.Arg1238Thr
XM_011535985.1:c.3533G>C	XP_011534287.1:p.Arg1178Thr
XM_011535986.1:c.3293G>C	XP_011534288.1:p.Arg1098Thr
XM_011535987.1:c.2912G>C	XP_011534289.1:p.Arg971Thr
XM_011535988.1:c.1775G>C	XP_011534290.1:p.Arg592Thr
NM_001346813.1:c.4634G>C	NP_001333742.1:p.Arg1545Thr
NM_001363725.1:c.2384G>C	NP_001350654.1:p.Arg795Thr
XM_011535984.2:c.4844G>C	XP_011534286.2:p.Arg1615Thr
XM_011535988.3:c.1775G>C	XP_011534290.1:p.Arg592Thr
XM_017011103.2:c.4745G>C	XP_016866592.1:p.Arg1582Thr
XM_017011104.1:c.4715G>C	XP_016866593.1:p.Arg1572Thr
XM_017011105.2:c.4685G>C	XP_016866594.1:p.Arg1562Thr
XM_017011106.2:c.4556G>C	XP_016866595.1:p.Arg1519Thr
XM_017011107.2:c.4535G>C	XP_016866596.1:p.Arg1512Thr
XR_002956289.1:n.4830G>C
NM_001363725.2:c.2384G>C	NP_001350654.1:p.Arg795Thr
NM_001371656.1:c.4763G>C	NP_001358585.1:p.Arg1588Thr
NM_001374820.1:c.4763G>C	NP_001361749.1:p.Arg1588Thr
NM_001374828.1:c.4883G>C MANE Select	NP_001361757.1:p.Arg1628Thr
NM_017519.3:c.4724G>C	NP_059989.3:p.Arg1575Thr