Canonical Allele Identifier: CA366242016

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4724G>T	ENSP00000055163.8:p.Arg1575Met
ENST00000414678.8:c.4793G>T	ENSP00000412835.3:p.Arg1598Met
ENST00000637015.2:c.5012G>T	ENSP00000489729.2:p.Arg1671Met
ENST00000346085.10:c.4763G>T	ENSP00000344546.5:p.Arg1588Met
ENST00000350026.10:c.4475G>T	ENSP00000055163.7:p.Arg1492Met
ENST00000414678.7:c.3041G>T	ENSP00000412835.2:p.Arg1014Met
ENST00000635849.1:c.2204G>T	ENSP00000490948.1:p.Arg735Met
ENST00000635957.1:c.1835G>T	ENSP00000490385.1:p.Arg612Met
ENST00000636227.1:n.3346G>T
ENST00000636254.1:n.803G>T
ENST00000636930.2:c.4883G>T MANE Select	ENSP00000490491.2:p.Arg1628Met
ENST00000636940.1:n.2880G>T
ENST00000637015.1:c.2251G>T
ENST00000637568.1:c.2165G>T
ENST00000637741.1:n.1549G>T
ENST00000637810.1:c.2225G>T	ENSP00000489636.1:p.Arg742Met
ENST00000637904.1:c.2384G>T	ENSP00000490550.1:p.Arg795Met
ENST00000647938.1:c.4514G>T	ENSP00000498155.1:p.Arg1505Met
ENST00000346085.9:c.4514G>T	ENSP00000344546.4:p.Arg1505Met
ENST00000350026.9:c.4475G>T	ENSP00000055163.7:p.Arg1492Met
ENST00000414678.6:c.3041G>T	ENSP00000412835.2:p.Arg1014Met
NM_017519.2:c.4475G>T	NP_059989.2:p.Arg1492Met
NM_020732.3:c.4514G>T	NP_065783.3:p.Arg1505Met
XM_005267069.3:c.4634G>T	XP_005267126.2:p.Arg1545Met
XM_011535984.1:c.3713G>T	XP_011534286.1:p.Arg1238Met
XM_011535985.1:c.3533G>T	XP_011534287.1:p.Arg1178Met
XM_011535986.1:c.3293G>T	XP_011534288.1:p.Arg1098Met
XM_011535987.1:c.2912G>T	XP_011534289.1:p.Arg971Met
XM_011535988.1:c.1775G>T	XP_011534290.1:p.Arg592Met
NM_001346813.1:c.4634G>T	NP_001333742.1:p.Arg1545Met
NM_001363725.1:c.2384G>T	NP_001350654.1:p.Arg795Met
XM_011535984.2:c.4844G>T	XP_011534286.2:p.Arg1615Met
XM_011535988.3:c.1775G>T	XP_011534290.1:p.Arg592Met
XM_017011103.2:c.4745G>T	XP_016866592.1:p.Arg1582Met
XM_017011104.1:c.4715G>T	XP_016866593.1:p.Arg1572Met
XM_017011105.2:c.4685G>T	XP_016866594.1:p.Arg1562Met
XM_017011106.2:c.4556G>T	XP_016866595.1:p.Arg1519Met
XM_017011107.2:c.4535G>T	XP_016866596.1:p.Arg1512Met
XR_002956289.1:n.4830G>T
NM_001363725.2:c.2384G>T	NP_001350654.1:p.Arg795Met
NM_001371656.1:c.4763G>T	NP_001358585.1:p.Arg1588Met
NM_001374820.1:c.4763G>T	NP_001361749.1:p.Arg1588Met
NM_001374828.1:c.4883G>T MANE Select	NP_001361757.1:p.Arg1628Met
NM_017519.3:c.4724G>T	NP_059989.3:p.Arg1575Met