Canonical Allele Identifier: CA366234359

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510904C>G (hg19) ; chr6:g.157189770C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189770C>G , CM000668.2:g.157189770C>G	GRCh38
NC_000006.11:g.157510904C>G , CM000668.1:g.157510904C>G	GRCh37
NC_000006.10:g.157552596C>G	NCBI36
NG_032093.1:g.416841C>G
NG_032093.2:g.416841C>G
NG_066624.1:g.418745C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3889C>G	ENSP00000055163.8:p.Gln1297Glu
ENST00000414678.8:c.3958C>G	ENSP00000412835.3:p.Gln1320Glu
ENST00000637015.2:c.4177C>G	ENSP00000489729.2:p.Gln1393Glu
ENST00000346085.10:c.3928C>G	ENSP00000344546.5:p.Gln1310Glu
ENST00000350026.10:c.3640C>G	ENSP00000055163.7:p.Gln1214Glu
ENST00000414678.7:c.2206C>G	ENSP00000412835.2:p.Gln736Glu
ENST00000635849.1:c.1369C>G	ENSP00000490948.1:p.Gln457Glu
ENST00000635957.1:c.1003C>G	ENSP00000490385.1:p.Gln335Glu
ENST00000636930.2:c.4048C>G MANE Select	ENSP00000490491.2:p.Gln1350Glu
ENST00000636940.1:n.2045C>G
ENST00000637015.1:c.1416C>G
ENST00000637568.1:c.1330C>G
ENST00000637741.1:n.714C>G
ENST00000637810.1:c.1390C>G	ENSP00000489636.1:p.Gln464Glu
ENST00000637904.1:c.1549C>G	ENSP00000490550.1:p.Gln517Glu
ENST00000647938.1:c.3679C>G	ENSP00000498155.1:p.Gln1227Glu
ENST00000346085.9:c.3679C>G	ENSP00000344546.4:p.Gln1227Glu
ENST00000350026.9:c.3640C>G	ENSP00000055163.7:p.Gln1214Glu
ENST00000414678.6:c.2206C>G	ENSP00000412835.2:p.Gln736Glu
NM_017519.2:c.3640C>G	NP_059989.2:p.Gln1214Glu
NM_020732.3:c.3679C>G	NP_065783.3:p.Gln1227Glu
XM_005267069.3:c.3799C>G	XP_005267126.2:p.Gln1267Glu
XM_011535984.1:c.2878C>G	XP_011534286.1:p.Gln960Glu
XM_011535985.1:c.2698C>G	XP_011534287.1:p.Gln900Glu
XM_011535986.1:c.2458C>G	XP_011534288.1:p.Gln820Glu
XM_011535987.1:c.2077C>G	XP_011534289.1:p.Gln693Glu
XM_011535988.1:c.940C>G	XP_011534290.1:p.Gln314Glu
NM_001346813.1:c.3799C>G	NP_001333742.1:p.Gln1267Glu
NM_001363725.1:c.1549C>G	NP_001350654.1:p.Gln517Glu
XM_011535984.2:c.4009C>G	XP_011534286.2:p.Gln1337Glu
XM_011535988.3:c.940C>G	XP_011534290.1:p.Gln314Glu
XM_017011103.2:c.3910C>G	XP_016866592.1:p.Gln1304Glu
XM_017011104.1:c.3880C>G	XP_016866593.1:p.Gln1294Glu
XM_017011105.2:c.3850C>G	XP_016866594.1:p.Gln1284Glu
XM_017011106.2:c.3721C>G	XP_016866595.1:p.Gln1241Glu
XM_017011107.2:c.3700C>G	XP_016866596.1:p.Gln1234Glu
XR_002956289.1:n.4092C>G
NM_001363725.2:c.1549C>G	NP_001350654.1:p.Gln517Glu
NM_001371656.1:c.3928C>G	NP_001358585.1:p.Gln1310Glu
NM_001374820.1:c.3928C>G	NP_001361749.1:p.Gln1310Glu
NM_001374828.1:c.4048C>G MANE Select	NP_001361757.1:p.Gln1350Glu
NM_017519.3:c.3889C>G	NP_059989.3:p.Gln1297Glu