Canonical Allele Identifier: CA452781520

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510828T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189694T>C , CM000668.2:g.157189694T>C	GRCh38
NC_000006.11:g.157510828T>C , CM000668.1:g.157510828T>C	GRCh37
NC_000006.10:g.157552520T>C	NCBI36
NG_032093.1:g.416765T>C
NG_032093.2:g.416765T>C
NG_066624.1:g.418669T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3813T>C	ENSP00000055163.8:p.Asn1271=
ENST00000414678.8:c.3882T>C	ENSP00000412835.3:p.Asn1294=
ENST00000637015.2:c.4101T>C	ENSP00000489729.2:p.Asn1367=
ENST00000346085.10:c.3852T>C	ENSP00000344546.5:p.Asn1284=
ENST00000350026.10:c.3564T>C	ENSP00000055163.7:p.Asn1188=
ENST00000414678.7:c.2130T>C	ENSP00000412835.2:p.Asn710=
ENST00000635849.1:c.1293T>C	ENSP00000490948.1:p.Asn431=
ENST00000635957.1:c.927T>C	ENSP00000490385.1:p.Asn309=
ENST00000636930.2:c.3972T>C MANE Select	ENSP00000490491.2:p.Asn1324=
ENST00000636940.1:n.1969T>C
ENST00000637015.1:c.1340T>C
ENST00000637568.1:c.1254T>C
ENST00000637741.1:n.638T>C
ENST00000637810.1:c.1314T>C	ENSP00000489636.1:p.Asn438=
ENST00000637904.1:c.1473T>C	ENSP00000490550.1:p.Asn491=
ENST00000647938.1:c.3603T>C	ENSP00000498155.1:p.Asn1201=
ENST00000346085.9:c.3603T>C	ENSP00000344546.4:p.Asn1201=
ENST00000350026.9:c.3564T>C	ENSP00000055163.7:p.Asn1188=
ENST00000414678.6:c.2130T>C	ENSP00000412835.2:p.Asn710=
NM_017519.2:c.3564T>C	NP_059989.2:p.Asn1188=
NM_020732.3:c.3603T>C	NP_065783.3:p.Asn1201=
XM_005267069.3:c.3723T>C	XP_005267126.2:p.Asn1241=
XM_011535984.1:c.2802T>C	XP_011534286.1:p.Asn934=
XM_011535985.1:c.2622T>C	XP_011534287.1:p.Asn874=
XM_011535986.1:c.2382T>C	XP_011534288.1:p.Asn794=
XM_011535987.1:c.2001T>C	XP_011534289.1:p.Asn667=
XM_011535988.1:c.864T>C	XP_011534290.1:p.Asn288=
NM_001346813.1:c.3723T>C	NP_001333742.1:p.Asn1241=
NM_001363725.1:c.1473T>C	NP_001350654.1:p.Asn491=
XM_011535984.2:c.3933T>C	XP_011534286.2:p.Asn1311=
XM_011535988.3:c.864T>C	XP_011534290.1:p.Asn288=
XM_017011103.2:c.3834T>C	XP_016866592.1:p.Asn1278=
XM_017011104.1:c.3804T>C	XP_016866593.1:p.Asn1268=
XM_017011105.2:c.3774T>C	XP_016866594.1:p.Asn1258=
XM_017011106.2:c.3645T>C	XP_016866595.1:p.Asn1215=
XM_017011107.2:c.3624T>C	XP_016866596.1:p.Asn1208=
XR_002956289.1:n.4016T>C
NM_001363725.2:c.1473T>C	NP_001350654.1:p.Asn491=
NM_001371656.1:c.3852T>C	NP_001358585.1:p.Asn1284=
NM_001374820.1:c.3852T>C	NP_001361749.1:p.Asn1284=
NM_001374828.1:c.3972T>C MANE Select	NP_001361757.1:p.Asn1324=
NM_017519.3:c.3813T>C	NP_059989.3:p.Asn1271=