Canonical Allele Identifier: CA452781488

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793217001
• MyVariant Identifiers: chr6:g.157510780C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189646C>T , CM000668.2:g.157189646C>T	GRCh38
NC_000006.11:g.157510780C>T , CM000668.1:g.157510780C>T	GRCh37
NC_000006.10:g.157552472C>T	NCBI36
NG_032093.1:g.416717C>T
NG_032093.2:g.416717C>T
NG_066624.1:g.418621C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3765C>T	ENSP00000055163.8:p.Asn1255=
ENST00000414678.8:c.3834C>T	ENSP00000412835.3:p.Asn1278=
ENST00000637015.2:c.4053C>T	ENSP00000489729.2:p.Asn1351=
ENST00000346085.10:c.3804C>T	ENSP00000344546.5:p.Asn1268=
ENST00000350026.10:c.3516C>T	ENSP00000055163.7:p.Asn1172=
ENST00000414678.7:c.2082C>T	ENSP00000412835.2:p.Asn694=
ENST00000635849.1:c.1245C>T	ENSP00000490948.1:p.Asn415=
ENST00000635957.1:c.879C>T	ENSP00000490385.1:p.Asn293=
ENST00000636930.2:c.3924C>T MANE Select	ENSP00000490491.2:p.Asn1308=
ENST00000636940.1:n.1921C>T
ENST00000637015.1:c.1292C>T
ENST00000637568.1:c.1206C>T
ENST00000637741.1:n.590C>T
ENST00000637810.1:c.1266C>T	ENSP00000489636.1:p.Asn422=
ENST00000637904.1:c.1425C>T	ENSP00000490550.1:p.Asn475=
ENST00000647938.1:c.3555C>T	ENSP00000498155.1:p.Asn1185=
ENST00000346085.9:c.3555C>T	ENSP00000344546.4:p.Asn1185=
ENST00000350026.9:c.3516C>T	ENSP00000055163.7:p.Asn1172=
ENST00000414678.6:c.2082C>T	ENSP00000412835.2:p.Asn694=
NM_017519.2:c.3516C>T	NP_059989.2:p.Asn1172=
NM_020732.3:c.3555C>T	NP_065783.3:p.Asn1185=
XM_005267069.3:c.3675C>T	XP_005267126.2:p.Asn1225=
XM_011535984.1:c.2754C>T	XP_011534286.1:p.Asn918=
XM_011535985.1:c.2574C>T	XP_011534287.1:p.Asn858=
XM_011535986.1:c.2334C>T	XP_011534288.1:p.Asn778=
XM_011535987.1:c.1953C>T	XP_011534289.1:p.Asn651=
XM_011535988.1:c.816C>T	XP_011534290.1:p.Asn272=
NM_001346813.1:c.3675C>T	NP_001333742.1:p.Asn1225=
NM_001363725.1:c.1425C>T	NP_001350654.1:p.Asn475=
XM_011535984.2:c.3885C>T	XP_011534286.2:p.Asn1295=
XM_011535988.3:c.816C>T	XP_011534290.1:p.Asn272=
XM_017011103.2:c.3786C>T	XP_016866592.1:p.Asn1262=
XM_017011104.1:c.3756C>T	XP_016866593.1:p.Asn1252=
XM_017011105.2:c.3726C>T	XP_016866594.1:p.Asn1242=
XM_017011106.2:c.3597C>T	XP_016866595.1:p.Asn1199=
XM_017011107.2:c.3576C>T	XP_016866596.1:p.Asn1192=
XR_002956289.1:n.3968C>T
NM_001363725.2:c.1425C>T	NP_001350654.1:p.Asn475=
NM_001371656.1:c.3804C>T	NP_001358585.1:p.Asn1268=
NM_001374820.1:c.3804C>T	NP_001361749.1:p.Asn1268=
NM_001374828.1:c.3924C>T MANE Select	NP_001361757.1:p.Asn1308=
NM_017519.3:c.3765C>T	NP_059989.3:p.Asn1255=