Canonical Allele Identifier: CA366241916

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522221A>T (hg19) ; chr6:g.157201087A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201087A>T , CM000668.2:g.157201087A>T	GRCh38
NC_000006.11:g.157522221A>T , CM000668.1:g.157522221A>T	GRCh37
NC_000006.10:g.157563913A>T	NCBI36
NG_032093.1:g.428158A>T
NG_032093.2:g.428158A>T
NG_066624.1:g.430062A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4703A>T	ENSP00000055163.8:p.Asp1568Val
ENST00000414678.8:c.4772A>T	ENSP00000412835.3:p.Asp1591Val
ENST00000637015.2:c.4991A>T	ENSP00000489729.2:p.Asp1664Val
ENST00000346085.10:c.4742A>T	ENSP00000344546.5:p.Asp1581Val
ENST00000350026.10:c.4454A>T	ENSP00000055163.7:p.Asp1485Val
ENST00000414678.7:c.3020A>T	ENSP00000412835.2:p.Asp1007Val
ENST00000635849.1:c.2183A>T	ENSP00000490948.1:p.Asp728Val
ENST00000635957.1:c.1814A>T	ENSP00000490385.1:p.Asp605Val
ENST00000636227.1:n.3325A>T
ENST00000636254.1:n.782A>T
ENST00000636930.2:c.4862A>T MANE Select	ENSP00000490491.2:p.Asp1621Val
ENST00000636940.1:n.2859A>T
ENST00000637015.1:c.2230A>T
ENST00000637568.1:c.2144A>T
ENST00000637741.1:n.1528A>T
ENST00000637810.1:c.2204A>T	ENSP00000489636.1:p.Asp735Val
ENST00000637904.1:c.2363A>T	ENSP00000490550.1:p.Asp788Val
ENST00000647938.1:c.4493A>T	ENSP00000498155.1:p.Asp1498Val
ENST00000346085.9:c.4493A>T	ENSP00000344546.4:p.Asp1498Val
ENST00000350026.9:c.4454A>T	ENSP00000055163.7:p.Asp1485Val
ENST00000414678.6:c.3020A>T	ENSP00000412835.2:p.Asp1007Val
NM_017519.2:c.4454A>T	NP_059989.2:p.Asp1485Val
NM_020732.3:c.4493A>T	NP_065783.3:p.Asp1498Val
XM_005267069.3:c.4613A>T	XP_005267126.2:p.Asp1538Val
XM_011535984.1:c.3692A>T	XP_011534286.1:p.Asp1231Val
XM_011535985.1:c.3512A>T	XP_011534287.1:p.Asp1171Val
XM_011535986.1:c.3272A>T	XP_011534288.1:p.Asp1091Val
XM_011535987.1:c.2891A>T	XP_011534289.1:p.Asp964Val
XM_011535988.1:c.1754A>T	XP_011534290.1:p.Asp585Val
NM_001346813.1:c.4613A>T	NP_001333742.1:p.Asp1538Val
NM_001363725.1:c.2363A>T	NP_001350654.1:p.Asp788Val
XM_011535984.2:c.4823A>T	XP_011534286.2:p.Asp1608Val
XM_011535988.3:c.1754A>T	XP_011534290.1:p.Asp585Val
XM_017011103.2:c.4724A>T	XP_016866592.1:p.Asp1575Val
XM_017011104.1:c.4694A>T	XP_016866593.1:p.Asp1565Val
XM_017011105.2:c.4664A>T	XP_016866594.1:p.Asp1555Val
XM_017011106.2:c.4535A>T	XP_016866595.1:p.Asp1512Val
XM_017011107.2:c.4514A>T	XP_016866596.1:p.Asp1505Val
XR_002956289.1:n.4809A>T
NM_001363725.2:c.2363A>T	NP_001350654.1:p.Asp788Val
NM_001371656.1:c.4742A>T	NP_001358585.1:p.Asp1581Val
NM_001374820.1:c.4742A>T	NP_001361749.1:p.Asp1581Val
NM_001374828.1:c.4862A>T MANE Select	NP_001361757.1:p.Asp1621Val
NM_017519.3:c.4703A>T	NP_059989.3:p.Asp1568Val