Canonical Allele Identifier: CA366234971

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511210T>G (hg19) ; chr6:g.157190076T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190076T>G , CM000668.2:g.157190076T>G	GRCh38
NC_000006.11:g.157511210T>G , CM000668.1:g.157511210T>G	GRCh37
NC_000006.10:g.157552902T>G	NCBI36
NG_032093.1:g.417147T>G
NG_032093.2:g.417147T>G
NG_066624.1:g.419051T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3938T>G	ENSP00000055163.8:p.Val1313Gly
ENST00000414678.8:c.4007T>G	ENSP00000412835.3:p.Val1336Gly
ENST00000637015.2:c.4226T>G	ENSP00000489729.2:p.Val1409Gly
ENST00000346085.10:c.3977T>G	ENSP00000344546.5:p.Val1326Gly
ENST00000350026.10:c.3689T>G	ENSP00000055163.7:p.Val1230Gly
ENST00000414678.7:c.2255T>G	ENSP00000412835.2:p.Val752Gly
ENST00000635849.1:c.1418T>G	ENSP00000490948.1:p.Val473Gly
ENST00000635957.1:c.1049T>G	ENSP00000490385.1:p.Val350Gly
ENST00000636930.2:c.4097T>G MANE Select	ENSP00000490491.2:p.Val1366Gly
ENST00000636940.1:n.2094T>G
ENST00000637015.1:c.1465T>G
ENST00000637568.1:c.1379T>G
ENST00000637741.1:n.763T>G
ENST00000637810.1:c.1439T>G	ENSP00000489636.1:p.Val480Gly
ENST00000637904.1:c.1598T>G	ENSP00000490550.1:p.Val533Gly
ENST00000647938.1:c.3728T>G	ENSP00000498155.1:p.Val1243Gly
ENST00000346085.9:c.3728T>G	ENSP00000344546.4:p.Val1243Gly
ENST00000350026.9:c.3689T>G	ENSP00000055163.7:p.Val1230Gly
ENST00000414678.6:c.2255T>G	ENSP00000412835.2:p.Val752Gly
NM_017519.2:c.3689T>G	NP_059989.2:p.Val1230Gly
NM_020732.3:c.3728T>G	NP_065783.3:p.Val1243Gly
XM_005267069.3:c.3848T>G	XP_005267126.2:p.Val1283Gly
XM_011535984.1:c.2927T>G	XP_011534286.1:p.Val976Gly
XM_011535985.1:c.2747T>G	XP_011534287.1:p.Val916Gly
XM_011535986.1:c.2507T>G	XP_011534288.1:p.Val836Gly
XM_011535987.1:c.2126T>G	XP_011534289.1:p.Val709Gly
XM_011535988.1:c.989T>G	XP_011534290.1:p.Val330Gly
NM_001346813.1:c.3848T>G	NP_001333742.1:p.Val1283Gly
NM_001363725.1:c.1598T>G	NP_001350654.1:p.Val533Gly
XM_011535984.2:c.4058T>G	XP_011534286.2:p.Val1353Gly
XM_011535988.3:c.989T>G	XP_011534290.1:p.Val330Gly
XM_017011103.2:c.3959T>G	XP_016866592.1:p.Val1320Gly
XM_017011104.1:c.3929T>G	XP_016866593.1:p.Val1310Gly
XM_017011105.2:c.3899T>G	XP_016866594.1:p.Val1300Gly
XM_017011106.2:c.3770T>G	XP_016866595.1:p.Val1257Gly
XM_017011107.2:c.3749T>G	XP_016866596.1:p.Val1250Gly
XR_002956289.1:n.4141T>G
NM_001363725.2:c.1598T>G	NP_001350654.1:p.Val533Gly
NM_001371656.1:c.3977T>G	NP_001358585.1:p.Val1326Gly
NM_001374820.1:c.3977T>G	NP_001361749.1:p.Val1326Gly
NM_001374828.1:c.4097T>G MANE Select	NP_001361757.1:p.Val1366Gly
NM_017519.3:c.3938T>G	NP_059989.3:p.Val1313Gly