Canonical Allele Identifier: CA366233998

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510779A>G (hg19) ; chr6:g.157189645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189645A>G , CM000668.2:g.157189645A>G	GRCh38
NC_000006.11:g.157510779A>G , CM000668.1:g.157510779A>G	GRCh37
NC_000006.10:g.157552471A>G	NCBI36
NG_032093.1:g.416716A>G
NG_032093.2:g.416716A>G
NG_066624.1:g.418620A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3764A>G	ENSP00000055163.8:p.Asn1255Ser
ENST00000414678.8:c.3833A>G	ENSP00000412835.3:p.Asn1278Ser
ENST00000637015.2:c.4052A>G	ENSP00000489729.2:p.Asn1351Ser
ENST00000346085.10:c.3803A>G	ENSP00000344546.5:p.Asn1268Ser
ENST00000350026.10:c.3515A>G	ENSP00000055163.7:p.Asn1172Ser
ENST00000414678.7:c.2081A>G	ENSP00000412835.2:p.Asn694Ser
ENST00000635849.1:c.1244A>G	ENSP00000490948.1:p.Asn415Ser
ENST00000635957.1:c.878A>G	ENSP00000490385.1:p.Asn293Ser
ENST00000636930.2:c.3923A>G MANE Select	ENSP00000490491.2:p.Asn1308Ser
ENST00000636940.1:n.1920A>G
ENST00000637015.1:c.1291A>G
ENST00000637568.1:c.1205A>G
ENST00000637741.1:n.589A>G
ENST00000637810.1:c.1265A>G	ENSP00000489636.1:p.Asn422Ser
ENST00000637904.1:c.1424A>G	ENSP00000490550.1:p.Asn475Ser
ENST00000647938.1:c.3554A>G	ENSP00000498155.1:p.Asn1185Ser
ENST00000346085.9:c.3554A>G	ENSP00000344546.4:p.Asn1185Ser
ENST00000350026.9:c.3515A>G	ENSP00000055163.7:p.Asn1172Ser
ENST00000414678.6:c.2081A>G	ENSP00000412835.2:p.Asn694Ser
NM_017519.2:c.3515A>G	NP_059989.2:p.Asn1172Ser
NM_020732.3:c.3554A>G	NP_065783.3:p.Asn1185Ser
XM_005267069.3:c.3674A>G	XP_005267126.2:p.Asn1225Ser
XM_011535984.1:c.2753A>G	XP_011534286.1:p.Asn918Ser
XM_011535985.1:c.2573A>G	XP_011534287.1:p.Asn858Ser
XM_011535986.1:c.2333A>G	XP_011534288.1:p.Asn778Ser
XM_011535987.1:c.1952A>G	XP_011534289.1:p.Asn651Ser
XM_011535988.1:c.815A>G	XP_011534290.1:p.Asn272Ser
NM_001346813.1:c.3674A>G	NP_001333742.1:p.Asn1225Ser
NM_001363725.1:c.1424A>G	NP_001350654.1:p.Asn475Ser
XM_011535984.2:c.3884A>G	XP_011534286.2:p.Asn1295Ser
XM_011535988.3:c.815A>G	XP_011534290.1:p.Asn272Ser
XM_017011103.2:c.3785A>G	XP_016866592.1:p.Asn1262Ser
XM_017011104.1:c.3755A>G	XP_016866593.1:p.Asn1252Ser
XM_017011105.2:c.3725A>G	XP_016866594.1:p.Asn1242Ser
XM_017011106.2:c.3596A>G	XP_016866595.1:p.Asn1199Ser
XM_017011107.2:c.3575A>G	XP_016866596.1:p.Asn1192Ser
XR_002956289.1:n.3967A>G
NM_001363725.2:c.1424A>G	NP_001350654.1:p.Asn475Ser
NM_001371656.1:c.3803A>G	NP_001358585.1:p.Asn1268Ser
NM_001374820.1:c.3803A>G	NP_001361749.1:p.Asn1268Ser
NM_001374828.1:c.3923A>G MANE Select	NP_001361757.1:p.Asn1308Ser
NM_017519.3:c.3764A>G	NP_059989.3:p.Asn1255Ser