Canonical Allele Identifier: CA452783930

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519975C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198841C>T , CM000668.2:g.157198841C>T	GRCh38
NC_000006.11:g.157519975C>T , CM000668.1:g.157519975C>T	GRCh37
NC_000006.10:g.157561667C>T	NCBI36
NG_032093.1:g.425912C>T
NG_032093.2:g.425912C>T
NG_066624.1:g.427816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4254C>T	ENSP00000055163.8:p.Gly1418=
ENST00000414678.8:c.4323C>T	ENSP00000412835.3:p.Gly1441=
ENST00000637015.2:c.4542C>T	ENSP00000489729.2:p.Gly1514=
ENST00000346085.10:c.4293C>T	ENSP00000344546.5:p.Gly1431=
ENST00000350026.10:c.4005C>T	ENSP00000055163.7:p.Gly1335=
ENST00000414678.7:c.2571C>T	ENSP00000412835.2:p.Gly857=
ENST00000635849.1:c.1734C>T	ENSP00000490948.1:p.Gly578=
ENST00000635957.1:c.1365C>T	ENSP00000490385.1:p.Gly455=
ENST00000636227.1:n.2876C>T
ENST00000636254.1:n.333C>T
ENST00000636930.2:c.4413C>T MANE Select	ENSP00000490491.2:p.Gly1471=
ENST00000636940.1:n.2410C>T
ENST00000637015.1:c.1781C>T
ENST00000637568.1:c.1695C>T
ENST00000637741.1:n.1079C>T
ENST00000637810.1:c.1755C>T	ENSP00000489636.1:p.Gly585=
ENST00000637904.1:c.1914C>T	ENSP00000490550.1:p.Gly638=
ENST00000647938.1:c.4044C>T	ENSP00000498155.1:p.Gly1348=
ENST00000346085.9:c.4044C>T	ENSP00000344546.4:p.Gly1348=
ENST00000350026.9:c.4005C>T	ENSP00000055163.7:p.Gly1335=
ENST00000414678.6:c.2571C>T	ENSP00000412835.2:p.Gly857=
NM_017519.2:c.4005C>T	NP_059989.2:p.Gly1335=
NM_020732.3:c.4044C>T	NP_065783.3:p.Gly1348=
XM_005267069.3:c.4164C>T	XP_005267126.2:p.Gly1388=
XM_011535984.1:c.3243C>T	XP_011534286.1:p.Gly1081=
XM_011535985.1:c.3063C>T	XP_011534287.1:p.Gly1021=
XM_011535986.1:c.2823C>T	XP_011534288.1:p.Gly941=
XM_011535987.1:c.2442C>T	XP_011534289.1:p.Gly814=
XM_011535988.1:c.1305C>T	XP_011534290.1:p.Gly435=
NM_001346813.1:c.4164C>T	NP_001333742.1:p.Gly1388=
NM_001363725.1:c.1914C>T	NP_001350654.1:p.Gly638=
XM_011535984.2:c.4374C>T	XP_011534286.2:p.Gly1458=
XM_011535988.3:c.1305C>T	XP_011534290.1:p.Gly435=
XM_017011103.2:c.4275C>T	XP_016866592.1:p.Gly1425=
XM_017011104.1:c.4245C>T	XP_016866593.1:p.Gly1415=
XM_017011105.2:c.4215C>T	XP_016866594.1:p.Gly1405=
XM_017011106.2:c.4086C>T	XP_016866595.1:p.Gly1362=
XM_017011107.2:c.4065C>T	XP_016866596.1:p.Gly1355=
XR_002956289.1:n.4427-1864C>T
NM_001363725.2:c.1914C>T	NP_001350654.1:p.Gly638=
NM_001371656.1:c.4293C>T	NP_001358585.1:p.Gly1431=
NM_001374820.1:c.4293C>T	NP_001361749.1:p.Gly1431=
NM_001374828.1:c.4413C>T MANE Select	NP_001361757.1:p.Gly1471=
NM_017519.3:c.4254C>T	NP_059989.3:p.Gly1418=