Canonical Allele Identifier: CA366234074

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510814T>C (hg19) ; chr6:g.157189680T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189680T>C , CM000668.2:g.157189680T>C	GRCh38
NC_000006.11:g.157510814T>C , CM000668.1:g.157510814T>C	GRCh37
NC_000006.10:g.157552506T>C	NCBI36
NG_032093.1:g.416751T>C
NG_032093.2:g.416751T>C
NG_066624.1:g.418655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3799T>C	ENSP00000055163.8:p.Ser1267Pro
ENST00000414678.8:c.3868T>C	ENSP00000412835.3:p.Ser1290Pro
ENST00000637015.2:c.4087T>C	ENSP00000489729.2:p.Ser1363Pro
ENST00000346085.10:c.3838T>C	ENSP00000344546.5:p.Ser1280Pro
ENST00000350026.10:c.3550T>C	ENSP00000055163.7:p.Ser1184Pro
ENST00000414678.7:c.2116T>C	ENSP00000412835.2:p.Ser706Pro
ENST00000635849.1:c.1279T>C	ENSP00000490948.1:p.Ser427Pro
ENST00000635957.1:c.913T>C	ENSP00000490385.1:p.Ser305Pro
ENST00000636930.2:c.3958T>C MANE Select	ENSP00000490491.2:p.Ser1320Pro
ENST00000636940.1:n.1955T>C
ENST00000637015.1:c.1326T>C
ENST00000637568.1:c.1240T>C
ENST00000637741.1:n.624T>C
ENST00000637810.1:c.1300T>C	ENSP00000489636.1:p.Ser434Pro
ENST00000637904.1:c.1459T>C	ENSP00000490550.1:p.Ser487Pro
ENST00000647938.1:c.3589T>C	ENSP00000498155.1:p.Ser1197Pro
ENST00000346085.9:c.3589T>C	ENSP00000344546.4:p.Ser1197Pro
ENST00000350026.9:c.3550T>C	ENSP00000055163.7:p.Ser1184Pro
ENST00000414678.6:c.2116T>C	ENSP00000412835.2:p.Ser706Pro
NM_017519.2:c.3550T>C	NP_059989.2:p.Ser1184Pro
NM_020732.3:c.3589T>C	NP_065783.3:p.Ser1197Pro
XM_005267069.3:c.3709T>C	XP_005267126.2:p.Ser1237Pro
XM_011535984.1:c.2788T>C	XP_011534286.1:p.Ser930Pro
XM_011535985.1:c.2608T>C	XP_011534287.1:p.Ser870Pro
XM_011535986.1:c.2368T>C	XP_011534288.1:p.Ser790Pro
XM_011535987.1:c.1987T>C	XP_011534289.1:p.Ser663Pro
XM_011535988.1:c.850T>C	XP_011534290.1:p.Ser284Pro
NM_001346813.1:c.3709T>C	NP_001333742.1:p.Ser1237Pro
NM_001363725.1:c.1459T>C	NP_001350654.1:p.Ser487Pro
XM_011535984.2:c.3919T>C	XP_011534286.2:p.Ser1307Pro
XM_011535988.3:c.850T>C	XP_011534290.1:p.Ser284Pro
XM_017011103.2:c.3820T>C	XP_016866592.1:p.Ser1274Pro
XM_017011104.1:c.3790T>C	XP_016866593.1:p.Ser1264Pro
XM_017011105.2:c.3760T>C	XP_016866594.1:p.Ser1254Pro
XM_017011106.2:c.3631T>C	XP_016866595.1:p.Ser1211Pro
XM_017011107.2:c.3610T>C	XP_016866596.1:p.Ser1204Pro
XR_002956289.1:n.4002T>C
NM_001363725.2:c.1459T>C	NP_001350654.1:p.Ser487Pro
NM_001371656.1:c.3838T>C	NP_001358585.1:p.Ser1280Pro
NM_001374820.1:c.3838T>C	NP_001361749.1:p.Ser1280Pro
NM_001374828.1:c.3958T>C MANE Select	NP_001361757.1:p.Ser1320Pro
NM_017519.3:c.3799T>C	NP_059989.3:p.Ser1267Pro