Canonical Allele Identifier: CA366234862

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511196C>G (hg19) ; chr6:g.157190062C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190062C>G , CM000668.2:g.157190062C>G	GRCh38
NC_000006.11:g.157511196C>G , CM000668.1:g.157511196C>G	GRCh37
NC_000006.10:g.157552888C>G	NCBI36
NG_032093.1:g.417133C>G
NG_032093.2:g.417133C>G
NG_066624.1:g.419037C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3924C>G	ENSP00000055163.8:p.Asp1308Glu
ENST00000414678.8:c.3993C>G	ENSP00000412835.3:p.Asp1331Glu
ENST00000637015.2:c.4212C>G	ENSP00000489729.2:p.Asp1404Glu
ENST00000346085.10:c.3963C>G	ENSP00000344546.5:p.Asp1321Glu
ENST00000350026.10:c.3675C>G	ENSP00000055163.7:p.Asp1225Glu
ENST00000414678.7:c.2241C>G	ENSP00000412835.2:p.Asp747Glu
ENST00000635849.1:c.1404C>G	ENSP00000490948.1:p.Asp468Glu
ENST00000635957.1:c.1035C>G	ENSP00000490385.1:p.Asp345Glu
ENST00000636930.2:c.4083C>G MANE Select	ENSP00000490491.2:p.Asp1361Glu
ENST00000636940.1:n.2080C>G
ENST00000637015.1:c.1451C>G
ENST00000637568.1:c.1365C>G
ENST00000637741.1:n.749C>G
ENST00000637810.1:c.1425C>G	ENSP00000489636.1:p.Asp475Glu
ENST00000637904.1:c.1584C>G	ENSP00000490550.1:p.Asp528Glu
ENST00000647938.1:c.3714C>G	ENSP00000498155.1:p.Asp1238Glu
ENST00000346085.9:c.3714C>G	ENSP00000344546.4:p.Asp1238Glu
ENST00000350026.9:c.3675C>G	ENSP00000055163.7:p.Asp1225Glu
ENST00000414678.6:c.2241C>G	ENSP00000412835.2:p.Asp747Glu
NM_017519.2:c.3675C>G	NP_059989.2:p.Asp1225Glu
NM_020732.3:c.3714C>G	NP_065783.3:p.Asp1238Glu
XM_005267069.3:c.3834C>G	XP_005267126.2:p.Asp1278Glu
XM_011535984.1:c.2913C>G	XP_011534286.1:p.Asp971Glu
XM_011535985.1:c.2733C>G	XP_011534287.1:p.Asp911Glu
XM_011535986.1:c.2493C>G	XP_011534288.1:p.Asp831Glu
XM_011535987.1:c.2112C>G	XP_011534289.1:p.Asp704Glu
XM_011535988.1:c.975C>G	XP_011534290.1:p.Asp325Glu
NM_001346813.1:c.3834C>G	NP_001333742.1:p.Asp1278Glu
NM_001363725.1:c.1584C>G	NP_001350654.1:p.Asp528Glu
XM_011535984.2:c.4044C>G	XP_011534286.2:p.Asp1348Glu
XM_011535988.3:c.975C>G	XP_011534290.1:p.Asp325Glu
XM_017011103.2:c.3945C>G	XP_016866592.1:p.Asp1315Glu
XM_017011104.1:c.3915C>G	XP_016866593.1:p.Asp1305Glu
XM_017011105.2:c.3885C>G	XP_016866594.1:p.Asp1295Glu
XM_017011106.2:c.3756C>G	XP_016866595.1:p.Asp1252Glu
XM_017011107.2:c.3735C>G	XP_016866596.1:p.Asp1245Glu
XR_002956289.1:n.4127C>G
NM_001363725.2:c.1584C>G	NP_001350654.1:p.Asp528Glu
NM_001371656.1:c.3963C>G	NP_001358585.1:p.Asp1321Glu
NM_001374820.1:c.3963C>G	NP_001361749.1:p.Asp1321Glu
NM_001374828.1:c.4083C>G MANE Select	NP_001361757.1:p.Asp1361Glu
NM_017519.3:c.3924C>G	NP_059989.3:p.Asp1308Glu