Canonical Allele Identifier: CA366241277

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522074G>T (hg19) ; chr6:g.157200940G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200940G>T , CM000668.2:g.157200940G>T	GRCh38
NC_000006.11:g.157522074G>T , CM000668.1:g.157522074G>T	GRCh37
NC_000006.10:g.157563766G>T	NCBI36
NG_032093.1:g.428011G>T
NG_032093.2:g.428011G>T
NG_066624.1:g.429915G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4556G>T	ENSP00000055163.8:p.Gly1519Val
ENST00000414678.8:c.4625G>T	ENSP00000412835.3:p.Gly1542Val
ENST00000637015.2:c.4844G>T	ENSP00000489729.2:p.Gly1615Val
ENST00000346085.10:c.4595G>T	ENSP00000344546.5:p.Gly1532Val
ENST00000350026.10:c.4307G>T	ENSP00000055163.7:p.Gly1436Val
ENST00000414678.7:c.2873G>T	ENSP00000412835.2:p.Gly958Val
ENST00000635849.1:c.2036G>T	ENSP00000490948.1:p.Gly679Val
ENST00000635957.1:c.1667G>T	ENSP00000490385.1:p.Gly556Val
ENST00000636227.1:n.3178G>T
ENST00000636254.1:n.635G>T
ENST00000636930.2:c.4715G>T MANE Select	ENSP00000490491.2:p.Gly1572Val
ENST00000636940.1:n.2712G>T
ENST00000637015.1:c.2083G>T
ENST00000637568.1:c.1997G>T
ENST00000637741.1:n.1381G>T
ENST00000637810.1:c.2057G>T	ENSP00000489636.1:p.Gly686Val
ENST00000637904.1:c.2216G>T	ENSP00000490550.1:p.Gly739Val
ENST00000647938.1:c.4346G>T	ENSP00000498155.1:p.Gly1449Val
ENST00000346085.9:c.4346G>T	ENSP00000344546.4:p.Gly1449Val
ENST00000350026.9:c.4307G>T	ENSP00000055163.7:p.Gly1436Val
ENST00000414678.6:c.2873G>T	ENSP00000412835.2:p.Gly958Val
NM_017519.2:c.4307G>T	NP_059989.2:p.Gly1436Val
NM_020732.3:c.4346G>T	NP_065783.3:p.Gly1449Val
XM_005267069.3:c.4466G>T	XP_005267126.2:p.Gly1489Val
XM_011535984.1:c.3545G>T	XP_011534286.1:p.Gly1182Val
XM_011535985.1:c.3365G>T	XP_011534287.1:p.Gly1122Val
XM_011535986.1:c.3125G>T	XP_011534288.1:p.Gly1042Val
XM_011535987.1:c.2744G>T	XP_011534289.1:p.Gly915Val
XM_011535988.1:c.1607G>T	XP_011534290.1:p.Gly536Val
NM_001346813.1:c.4466G>T	NP_001333742.1:p.Gly1489Val
NM_001363725.1:c.2216G>T	NP_001350654.1:p.Gly739Val
XM_011535984.2:c.4676G>T	XP_011534286.2:p.Gly1559Val
XM_011535988.3:c.1607G>T	XP_011534290.1:p.Gly536Val
XM_017011103.2:c.4577G>T	XP_016866592.1:p.Gly1526Val
XM_017011104.1:c.4547G>T	XP_016866593.1:p.Gly1516Val
XM_017011105.2:c.4517G>T	XP_016866594.1:p.Gly1506Val
XM_017011106.2:c.4388G>T	XP_016866595.1:p.Gly1463Val
XM_017011107.2:c.4367G>T	XP_016866596.1:p.Gly1456Val
XR_002956289.1:n.4662G>T
NM_001363725.2:c.2216G>T	NP_001350654.1:p.Gly739Val
NM_001371656.1:c.4595G>T	NP_001358585.1:p.Gly1532Val
NM_001374820.1:c.4595G>T	NP_001361749.1:p.Gly1532Val
NM_001374828.1:c.4715G>T MANE Select	NP_001361757.1:p.Gly1572Val
NM_017519.3:c.4556G>T	NP_059989.3:p.Gly1519Val