Canonical Allele Identifier: CA366242070

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522264G>T (hg19) ; chr6:g.157201130G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201130G>T , CM000668.2:g.157201130G>T	GRCh38
NC_000006.11:g.157522264G>T , CM000668.1:g.157522264G>T	GRCh37
NC_000006.10:g.157563956G>T	NCBI36
NG_032093.1:g.428201G>T
NG_032093.2:g.428201G>T
NG_066624.1:g.430105G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4746G>T	ENSP00000055163.8:p.Trp1582Cys
ENST00000414678.8:c.4815G>T	ENSP00000412835.3:p.Trp1605Cys
ENST00000637015.2:c.5034G>T	ENSP00000489729.2:p.Trp1678Cys
ENST00000346085.10:c.4785G>T	ENSP00000344546.5:p.Trp1595Cys
ENST00000350026.10:c.4497G>T	ENSP00000055163.7:p.Trp1499Cys
ENST00000414678.7:c.3063G>T	ENSP00000412835.2:p.Trp1021Cys
ENST00000635849.1:c.2226G>T	ENSP00000490948.1:p.Trp742Cys
ENST00000635957.1:c.1857G>T	ENSP00000490385.1:p.Trp619Cys
ENST00000636227.1:n.3368G>T
ENST00000636254.1:n.825G>T
ENST00000636930.2:c.4905G>T MANE Select	ENSP00000490491.2:p.Trp1635Cys
ENST00000636940.1:n.2902G>T
ENST00000637015.1:c.2273G>T
ENST00000637568.1:c.2187G>T
ENST00000637741.1:n.1571G>T
ENST00000637810.1:c.2247G>T	ENSP00000489636.1:p.Trp749Cys
ENST00000637904.1:c.2406G>T	ENSP00000490550.1:p.Trp802Cys
ENST00000647938.1:c.4536G>T	ENSP00000498155.1:p.Trp1512Cys
ENST00000346085.9:c.4536G>T	ENSP00000344546.4:p.Trp1512Cys
ENST00000350026.9:c.4497G>T	ENSP00000055163.7:p.Trp1499Cys
ENST00000414678.6:c.3063G>T	ENSP00000412835.2:p.Trp1021Cys
NM_017519.2:c.4497G>T	NP_059989.2:p.Trp1499Cys
NM_020732.3:c.4536G>T	NP_065783.3:p.Trp1512Cys
XM_005267069.3:c.4656G>T	XP_005267126.2:p.Trp1552Cys
XM_011535984.1:c.3735G>T	XP_011534286.1:p.Trp1245Cys
XM_011535985.1:c.3555G>T	XP_011534287.1:p.Trp1185Cys
XM_011535986.1:c.3315G>T	XP_011534288.1:p.Trp1105Cys
XM_011535987.1:c.2934G>T	XP_011534289.1:p.Trp978Cys
XM_011535988.1:c.1797G>T	XP_011534290.1:p.Trp599Cys
NM_001346813.1:c.4656G>T	NP_001333742.1:p.Trp1552Cys
NM_001363725.1:c.2406G>T	NP_001350654.1:p.Trp802Cys
XM_011535984.2:c.4866G>T	XP_011534286.2:p.Trp1622Cys
XM_011535988.3:c.1797G>T	XP_011534290.1:p.Trp599Cys
XM_017011103.2:c.4767G>T	XP_016866592.1:p.Trp1589Cys
XM_017011104.1:c.4737G>T	XP_016866593.1:p.Trp1579Cys
XM_017011105.2:c.4707G>T	XP_016866594.1:p.Trp1569Cys
XM_017011106.2:c.4578G>T	XP_016866595.1:p.Trp1526Cys
XM_017011107.2:c.4557G>T	XP_016866596.1:p.Trp1519Cys
XR_002956289.1:n.4852G>T
NM_001363725.2:c.2406G>T	NP_001350654.1:p.Trp802Cys
NM_001371656.1:c.4785G>T	NP_001358585.1:p.Trp1595Cys
NM_001374820.1:c.4785G>T	NP_001361749.1:p.Trp1595Cys
NM_001374828.1:c.4905G>T MANE Select	NP_001361757.1:p.Trp1635Cys
NM_017519.3:c.4746G>T	NP_059989.3:p.Trp1582Cys