Canonical Allele Identifier: CA366241326

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522100G>C (hg19) ; chr6:g.157200966G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200966G>C , CM000668.2:g.157200966G>C	GRCh38
NC_000006.11:g.157522100G>C , CM000668.1:g.157522100G>C	GRCh37
NC_000006.10:g.157563792G>C	NCBI36
NG_032093.1:g.428037G>C
NG_032093.2:g.428037G>C
NG_066624.1:g.429941G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4582G>C	ENSP00000055163.8:p.Glu1528Gln
ENST00000414678.8:c.4651G>C	ENSP00000412835.3:p.Glu1551Gln
ENST00000637015.2:c.4870G>C	ENSP00000489729.2:p.Glu1624Gln
ENST00000346085.10:c.4621G>C	ENSP00000344546.5:p.Glu1541Gln
ENST00000350026.10:c.4333G>C	ENSP00000055163.7:p.Glu1445Gln
ENST00000414678.7:c.2899G>C	ENSP00000412835.2:p.Glu967Gln
ENST00000635849.1:c.2062G>C	ENSP00000490948.1:p.Glu688Gln
ENST00000635957.1:c.1693G>C	ENSP00000490385.1:p.Glu565Gln
ENST00000636227.1:n.3204G>C
ENST00000636254.1:n.661G>C
ENST00000636930.2:c.4741G>C MANE Select	ENSP00000490491.2:p.Glu1581Gln
ENST00000636940.1:n.2738G>C
ENST00000637015.1:c.2109G>C
ENST00000637568.1:c.2023G>C
ENST00000637741.1:n.1407G>C
ENST00000637810.1:c.2083G>C	ENSP00000489636.1:p.Glu695Gln
ENST00000637904.1:c.2242G>C	ENSP00000490550.1:p.Glu748Gln
ENST00000647938.1:c.4372G>C	ENSP00000498155.1:p.Glu1458Gln
ENST00000346085.9:c.4372G>C	ENSP00000344546.4:p.Glu1458Gln
ENST00000350026.9:c.4333G>C	ENSP00000055163.7:p.Glu1445Gln
ENST00000414678.6:c.2899G>C	ENSP00000412835.2:p.Glu967Gln
NM_017519.2:c.4333G>C	NP_059989.2:p.Glu1445Gln
NM_020732.3:c.4372G>C	NP_065783.3:p.Glu1458Gln
XM_005267069.3:c.4492G>C	XP_005267126.2:p.Glu1498Gln
XM_011535984.1:c.3571G>C	XP_011534286.1:p.Glu1191Gln
XM_011535985.1:c.3391G>C	XP_011534287.1:p.Glu1131Gln
XM_011535986.1:c.3151G>C	XP_011534288.1:p.Glu1051Gln
XM_011535987.1:c.2770G>C	XP_011534289.1:p.Glu924Gln
XM_011535988.1:c.1633G>C	XP_011534290.1:p.Glu545Gln
NM_001346813.1:c.4492G>C	NP_001333742.1:p.Glu1498Gln
NM_001363725.1:c.2242G>C	NP_001350654.1:p.Glu748Gln
XM_011535984.2:c.4702G>C	XP_011534286.2:p.Glu1568Gln
XM_011535988.3:c.1633G>C	XP_011534290.1:p.Glu545Gln
XM_017011103.2:c.4603G>C	XP_016866592.1:p.Glu1535Gln
XM_017011104.1:c.4573G>C	XP_016866593.1:p.Glu1525Gln
XM_017011105.2:c.4543G>C	XP_016866594.1:p.Glu1515Gln
XM_017011106.2:c.4414G>C	XP_016866595.1:p.Glu1472Gln
XM_017011107.2:c.4393G>C	XP_016866596.1:p.Glu1465Gln
XR_002956289.1:n.4688G>C
NM_001363725.2:c.2242G>C	NP_001350654.1:p.Glu748Gln
NM_001371656.1:c.4621G>C	NP_001358585.1:p.Glu1541Gln
NM_001374820.1:c.4621G>C	NP_001361749.1:p.Glu1541Gln
NM_001374828.1:c.4741G>C MANE Select	NP_001361757.1:p.Glu1581Gln
NM_017519.3:c.4582G>C	NP_059989.3:p.Glu1528Gln