Canonical Allele Identifier: CA366242001

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522236A>T (hg19) ; chr6:g.157201102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201102A>T , CM000668.2:g.157201102A>T	GRCh38
NC_000006.11:g.157522236A>T , CM000668.1:g.157522236A>T	GRCh37
NC_000006.10:g.157563928A>T	NCBI36
NG_032093.1:g.428173A>T
NG_032093.2:g.428173A>T
NG_066624.1:g.430077A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4718A>T	ENSP00000055163.8:p.Asp1573Val
ENST00000414678.8:c.4787A>T	ENSP00000412835.3:p.Asp1596Val
ENST00000637015.2:c.5006A>T	ENSP00000489729.2:p.Asp1669Val
ENST00000346085.10:c.4757A>T	ENSP00000344546.5:p.Asp1586Val
ENST00000350026.10:c.4469A>T	ENSP00000055163.7:p.Asp1490Val
ENST00000414678.7:c.3035A>T	ENSP00000412835.2:p.Asp1012Val
ENST00000635849.1:c.2198A>T	ENSP00000490948.1:p.Asp733Val
ENST00000635957.1:c.1829A>T	ENSP00000490385.1:p.Asp610Val
ENST00000636227.1:n.3340A>T
ENST00000636254.1:n.797A>T
ENST00000636930.2:c.4877A>T MANE Select	ENSP00000490491.2:p.Asp1626Val
ENST00000636940.1:n.2874A>T
ENST00000637015.1:c.2245A>T
ENST00000637568.1:c.2159A>T
ENST00000637741.1:n.1543A>T
ENST00000637810.1:c.2219A>T	ENSP00000489636.1:p.Asp740Val
ENST00000637904.1:c.2378A>T	ENSP00000490550.1:p.Asp793Val
ENST00000647938.1:c.4508A>T	ENSP00000498155.1:p.Asp1503Val
ENST00000346085.9:c.4508A>T	ENSP00000344546.4:p.Asp1503Val
ENST00000350026.9:c.4469A>T	ENSP00000055163.7:p.Asp1490Val
ENST00000414678.6:c.3035A>T	ENSP00000412835.2:p.Asp1012Val
NM_017519.2:c.4469A>T	NP_059989.2:p.Asp1490Val
NM_020732.3:c.4508A>T	NP_065783.3:p.Asp1503Val
XM_005267069.3:c.4628A>T	XP_005267126.2:p.Asp1543Val
XM_011535984.1:c.3707A>T	XP_011534286.1:p.Asp1236Val
XM_011535985.1:c.3527A>T	XP_011534287.1:p.Asp1176Val
XM_011535986.1:c.3287A>T	XP_011534288.1:p.Asp1096Val
XM_011535987.1:c.2906A>T	XP_011534289.1:p.Asp969Val
XM_011535988.1:c.1769A>T	XP_011534290.1:p.Asp590Val
NM_001346813.1:c.4628A>T	NP_001333742.1:p.Asp1543Val
NM_001363725.1:c.2378A>T	NP_001350654.1:p.Asp793Val
XM_011535984.2:c.4838A>T	XP_011534286.2:p.Asp1613Val
XM_011535988.3:c.1769A>T	XP_011534290.1:p.Asp590Val
XM_017011103.2:c.4739A>T	XP_016866592.1:p.Asp1580Val
XM_017011104.1:c.4709A>T	XP_016866593.1:p.Asp1570Val
XM_017011105.2:c.4679A>T	XP_016866594.1:p.Asp1560Val
XM_017011106.2:c.4550A>T	XP_016866595.1:p.Asp1517Val
XM_017011107.2:c.4529A>T	XP_016866596.1:p.Asp1510Val
XR_002956289.1:n.4824A>T
NM_001363725.2:c.2378A>T	NP_001350654.1:p.Asp793Val
NM_001371656.1:c.4757A>T	NP_001358585.1:p.Asp1586Val
NM_001374820.1:c.4757A>T	NP_001361749.1:p.Asp1586Val
NM_001374828.1:c.4877A>T MANE Select	NP_001361757.1:p.Asp1626Val
NM_017519.3:c.4718A>T	NP_059989.3:p.Asp1573Val