Canonical Allele Identifier: CA366235317

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511255C>G (hg19) ; chr6:g.157190121C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190121C>G , CM000668.2:g.157190121C>G	GRCh38
NC_000006.11:g.157511255C>G , CM000668.1:g.157511255C>G	GRCh37
NC_000006.10:g.157552947C>G	NCBI36
NG_032093.1:g.417192C>G
NG_032093.2:g.417192C>G
NG_066624.1:g.419096C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3983C>G	ENSP00000055163.8:p.Ala1328Gly
ENST00000414678.8:c.4052C>G	ENSP00000412835.3:p.Ala1351Gly
ENST00000637015.2:c.4271C>G	ENSP00000489729.2:p.Ala1424Gly
ENST00000346085.10:c.4022C>G	ENSP00000344546.5:p.Ala1341Gly
ENST00000350026.10:c.3734C>G	ENSP00000055163.7:p.Ala1245Gly
ENST00000414678.7:c.2300C>G	ENSP00000412835.2:p.Ala767Gly
ENST00000635849.1:c.1463C>G	ENSP00000490948.1:p.Ala488Gly
ENST00000635957.1:c.1094C>G	ENSP00000490385.1:p.Ala365Gly
ENST00000636930.2:c.4142C>G MANE Select	ENSP00000490491.2:p.Ala1381Gly
ENST00000636940.1:n.2139C>G
ENST00000637015.1:c.1510C>G
ENST00000637568.1:c.1424C>G
ENST00000637741.1:n.808C>G
ENST00000637810.1:c.1484C>G	ENSP00000489636.1:p.Ala495Gly
ENST00000637904.1:c.1643C>G	ENSP00000490550.1:p.Ala548Gly
ENST00000647938.1:c.3773C>G	ENSP00000498155.1:p.Ala1258Gly
ENST00000346085.9:c.3773C>G	ENSP00000344546.4:p.Ala1258Gly
ENST00000350026.9:c.3734C>G	ENSP00000055163.7:p.Ala1245Gly
ENST00000414678.6:c.2300C>G	ENSP00000412835.2:p.Ala767Gly
NM_017519.2:c.3734C>G	NP_059989.2:p.Ala1245Gly
NM_020732.3:c.3773C>G	NP_065783.3:p.Ala1258Gly
XM_005267069.3:c.3893C>G	XP_005267126.2:p.Ala1298Gly
XM_011535984.1:c.2972C>G	XP_011534286.1:p.Ala991Gly
XM_011535985.1:c.2792C>G	XP_011534287.1:p.Ala931Gly
XM_011535986.1:c.2552C>G	XP_011534288.1:p.Ala851Gly
XM_011535987.1:c.2171C>G	XP_011534289.1:p.Ala724Gly
XM_011535988.1:c.1034C>G	XP_011534290.1:p.Ala345Gly
NM_001346813.1:c.3893C>G	NP_001333742.1:p.Ala1298Gly
NM_001363725.1:c.1643C>G	NP_001350654.1:p.Ala548Gly
XM_011535984.2:c.4103C>G	XP_011534286.2:p.Ala1368Gly
XM_011535988.3:c.1034C>G	XP_011534290.1:p.Ala345Gly
XM_017011103.2:c.4004C>G	XP_016866592.1:p.Ala1335Gly
XM_017011104.1:c.3974C>G	XP_016866593.1:p.Ala1325Gly
XM_017011105.2:c.3944C>G	XP_016866594.1:p.Ala1315Gly
XM_017011106.2:c.3815C>G	XP_016866595.1:p.Ala1272Gly
XM_017011107.2:c.3794C>G	XP_016866596.1:p.Ala1265Gly
XR_002956289.1:n.4186C>G
NM_001363725.2:c.1643C>G	NP_001350654.1:p.Ala548Gly
NM_001371656.1:c.4022C>G	NP_001358585.1:p.Ala1341Gly
NM_001374820.1:c.4022C>G	NP_001361749.1:p.Ala1341Gly
NM_001374828.1:c.4142C>G MANE Select	NP_001361757.1:p.Ala1381Gly
NM_017519.3:c.3983C>G	NP_059989.3:p.Ala1328Gly