Canonical Allele Identifier: CA452977874

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522003T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200869T>C , CM000668.2:g.157200869T>C	GRCh38
NC_000006.11:g.157522003T>C , CM000668.1:g.157522003T>C	GRCh37
NC_000006.10:g.157563695T>C	NCBI36
NG_032093.1:g.427940T>C
NG_032093.2:g.427940T>C
NG_066624.1:g.429844T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4485T>C	ENSP00000055163.8:p.Tyr1495=
ENST00000414678.8:c.4554T>C	ENSP00000412835.3:p.Tyr1518=
ENST00000637015.2:c.4773T>C	ENSP00000489729.2:p.Tyr1591=
ENST00000346085.10:c.4524T>C	ENSP00000344546.5:p.Tyr1508=
ENST00000350026.10:c.4236T>C	ENSP00000055163.7:p.Tyr1412=
ENST00000414678.7:c.2802T>C	ENSP00000412835.2:p.Tyr934=
ENST00000635849.1:c.1965T>C	ENSP00000490948.1:p.Tyr655=
ENST00000635957.1:c.1596T>C	ENSP00000490385.1:p.Tyr532=
ENST00000636227.1:n.3107T>C
ENST00000636254.1:n.564T>C
ENST00000636930.2:c.4644T>C MANE Select	ENSP00000490491.2:p.Tyr1548=
ENST00000636940.1:n.2641T>C
ENST00000637015.1:c.2012T>C
ENST00000637568.1:c.1926T>C
ENST00000637741.1:n.1310T>C
ENST00000637810.1:c.1986T>C	ENSP00000489636.1:p.Tyr662=
ENST00000637904.1:c.2145T>C	ENSP00000490550.1:p.Tyr715=
ENST00000647938.1:c.4275T>C	ENSP00000498155.1:p.Tyr1425=
ENST00000346085.9:c.4275T>C	ENSP00000344546.4:p.Tyr1425=
ENST00000350026.9:c.4236T>C	ENSP00000055163.7:p.Tyr1412=
ENST00000414678.6:c.2802T>C	ENSP00000412835.2:p.Tyr934=
NM_017519.2:c.4236T>C	NP_059989.2:p.Tyr1412=
NM_020732.3:c.4275T>C	NP_065783.3:p.Tyr1425=
XM_005267069.3:c.4395T>C	XP_005267126.2:p.Tyr1465=
XM_011535984.1:c.3474T>C	XP_011534286.1:p.Tyr1158=
XM_011535985.1:c.3294T>C	XP_011534287.1:p.Tyr1098=
XM_011535986.1:c.3054T>C	XP_011534288.1:p.Tyr1018=
XM_011535987.1:c.2673T>C	XP_011534289.1:p.Tyr891=
XM_011535988.1:c.1536T>C	XP_011534290.1:p.Tyr512=
NM_001346813.1:c.4395T>C	NP_001333742.1:p.Tyr1465=
NM_001363725.1:c.2145T>C	NP_001350654.1:p.Tyr715=
XM_011535984.2:c.4605T>C	XP_011534286.2:p.Tyr1535=
XM_011535988.3:c.1536T>C	XP_011534290.1:p.Tyr512=
XM_017011103.2:c.4506T>C	XP_016866592.1:p.Tyr1502=
XM_017011104.1:c.4476T>C	XP_016866593.1:p.Tyr1492=
XM_017011105.2:c.4446T>C	XP_016866594.1:p.Tyr1482=
XM_017011106.2:c.4317T>C	XP_016866595.1:p.Tyr1439=
XM_017011107.2:c.4296T>C	XP_016866596.1:p.Tyr1432=
XR_002956289.1:n.4591T>C
NM_001363725.2:c.2145T>C	NP_001350654.1:p.Tyr715=
NM_001371656.1:c.4524T>C	NP_001358585.1:p.Tyr1508=
NM_001374820.1:c.4524T>C	NP_001361749.1:p.Tyr1508=
NM_001374828.1:c.4644T>C MANE Select	NP_001361757.1:p.Tyr1548=
NM_017519.3:c.4485T>C	NP_059989.3:p.Tyr1495=