Canonical Allele Identifier: CA366241491

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522146A>C (hg19) ; chr6:g.157201012A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201012A>C , CM000668.2:g.157201012A>C	GRCh38
NC_000006.11:g.157522146A>C , CM000668.1:g.157522146A>C	GRCh37
NC_000006.10:g.157563838A>C	NCBI36
NG_032093.1:g.428083A>C
NG_032093.2:g.428083A>C
NG_066624.1:g.429987A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4628A>C	ENSP00000055163.8:p.Tyr1543Ser
ENST00000414678.8:c.4697A>C	ENSP00000412835.3:p.Tyr1566Ser
ENST00000637015.2:c.4916A>C	ENSP00000489729.2:p.Tyr1639Ser
ENST00000346085.10:c.4667A>C	ENSP00000344546.5:p.Tyr1556Ser
ENST00000350026.10:c.4379A>C	ENSP00000055163.7:p.Tyr1460Ser
ENST00000414678.7:c.2945A>C	ENSP00000412835.2:p.Tyr982Ser
ENST00000635849.1:c.2108A>C	ENSP00000490948.1:p.Tyr703Ser
ENST00000635957.1:c.1739A>C	ENSP00000490385.1:p.Tyr580Ser
ENST00000636227.1:n.3250A>C
ENST00000636254.1:n.707A>C
ENST00000636930.2:c.4787A>C MANE Select	ENSP00000490491.2:p.Tyr1596Ser
ENST00000636940.1:n.2784A>C
ENST00000637015.1:c.2155A>C
ENST00000637568.1:c.2069A>C
ENST00000637741.1:n.1453A>C
ENST00000637810.1:c.2129A>C	ENSP00000489636.1:p.Tyr710Ser
ENST00000637904.1:c.2288A>C	ENSP00000490550.1:p.Tyr763Ser
ENST00000647938.1:c.4418A>C	ENSP00000498155.1:p.Tyr1473Ser
ENST00000346085.9:c.4418A>C	ENSP00000344546.4:p.Tyr1473Ser
ENST00000350026.9:c.4379A>C	ENSP00000055163.7:p.Tyr1460Ser
ENST00000414678.6:c.2945A>C	ENSP00000412835.2:p.Tyr982Ser
NM_017519.2:c.4379A>C	NP_059989.2:p.Tyr1460Ser
NM_020732.3:c.4418A>C	NP_065783.3:p.Tyr1473Ser
XM_005267069.3:c.4538A>C	XP_005267126.2:p.Tyr1513Ser
XM_011535984.1:c.3617A>C	XP_011534286.1:p.Tyr1206Ser
XM_011535985.1:c.3437A>C	XP_011534287.1:p.Tyr1146Ser
XM_011535986.1:c.3197A>C	XP_011534288.1:p.Tyr1066Ser
XM_011535987.1:c.2816A>C	XP_011534289.1:p.Tyr939Ser
XM_011535988.1:c.1679A>C	XP_011534290.1:p.Tyr560Ser
NM_001346813.1:c.4538A>C	NP_001333742.1:p.Tyr1513Ser
NM_001363725.1:c.2288A>C	NP_001350654.1:p.Tyr763Ser
XM_011535984.2:c.4748A>C	XP_011534286.2:p.Tyr1583Ser
XM_011535988.3:c.1679A>C	XP_011534290.1:p.Tyr560Ser
XM_017011103.2:c.4649A>C	XP_016866592.1:p.Tyr1550Ser
XM_017011104.1:c.4619A>C	XP_016866593.1:p.Tyr1540Ser
XM_017011105.2:c.4589A>C	XP_016866594.1:p.Tyr1530Ser
XM_017011106.2:c.4460A>C	XP_016866595.1:p.Tyr1487Ser
XM_017011107.2:c.4439A>C	XP_016866596.1:p.Tyr1480Ser
XR_002956289.1:n.4734A>C
NM_001363725.2:c.2288A>C	NP_001350654.1:p.Tyr763Ser
NM_001371656.1:c.4667A>C	NP_001358585.1:p.Tyr1556Ser
NM_001374820.1:c.4667A>C	NP_001361749.1:p.Tyr1556Ser
NM_001374828.1:c.4787A>C MANE Select	NP_001361757.1:p.Tyr1596Ser
NM_017519.3:c.4628A>C	NP_059989.3:p.Tyr1543Ser