Canonical Allele Identifier: CA366241327

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235703
• MyVariant Identifiers: chr6:g.157522100G>T (hg19) ; chr6:g.157200966G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4582G>T	ENSP00000055163.8:p.Glu1528Ter
ENST00000414678.8:c.4651G>T	ENSP00000412835.3:p.Glu1551Ter
ENST00000637015.2:c.4870G>T	ENSP00000489729.2:p.Glu1624Ter
ENST00000346085.10:c.4621G>T	ENSP00000344546.5:p.Glu1541Ter
ENST00000350026.10:c.4333G>T	ENSP00000055163.7:p.Glu1445Ter
ENST00000414678.7:c.2899G>T	ENSP00000412835.2:p.Glu967Ter
ENST00000635849.1:c.2062G>T	ENSP00000490948.1:p.Glu688Ter
ENST00000635957.1:c.1693G>T	ENSP00000490385.1:p.Glu565Ter
ENST00000636227.1:n.3204G>T
ENST00000636254.1:n.661G>T
ENST00000636930.2:c.4741G>T MANE Select	ENSP00000490491.2:p.Glu1581Ter
ENST00000636940.1:n.2738G>T
ENST00000637015.1:c.2109G>T
ENST00000637568.1:c.2023G>T
ENST00000637741.1:n.1407G>T
ENST00000637810.1:c.2083G>T	ENSP00000489636.1:p.Glu695Ter
ENST00000637904.1:c.2242G>T	ENSP00000490550.1:p.Glu748Ter
ENST00000647938.1:c.4372G>T	ENSP00000498155.1:p.Glu1458Ter
ENST00000346085.9:c.4372G>T	ENSP00000344546.4:p.Glu1458Ter
ENST00000350026.9:c.4333G>T	ENSP00000055163.7:p.Glu1445Ter
ENST00000414678.6:c.2899G>T	ENSP00000412835.2:p.Glu967Ter
NM_017519.2:c.4333G>T	NP_059989.2:p.Glu1445Ter
NM_020732.3:c.4372G>T	NP_065783.3:p.Glu1458Ter
XM_005267069.3:c.4492G>T	XP_005267126.2:p.Glu1498Ter
XM_011535984.1:c.3571G>T	XP_011534286.1:p.Glu1191Ter
XM_011535985.1:c.3391G>T	XP_011534287.1:p.Glu1131Ter
XM_011535986.1:c.3151G>T	XP_011534288.1:p.Glu1051Ter
XM_011535987.1:c.2770G>T	XP_011534289.1:p.Glu924Ter
XM_011535988.1:c.1633G>T	XP_011534290.1:p.Glu545Ter
NM_001346813.1:c.4492G>T	NP_001333742.1:p.Glu1498Ter
NM_001363725.1:c.2242G>T	NP_001350654.1:p.Glu748Ter
XM_011535984.2:c.4702G>T	XP_011534286.2:p.Glu1568Ter
XM_011535988.3:c.1633G>T	XP_011534290.1:p.Glu545Ter
XM_017011103.2:c.4603G>T	XP_016866592.1:p.Glu1535Ter
XM_017011104.1:c.4573G>T	XP_016866593.1:p.Glu1525Ter
XM_017011105.2:c.4543G>T	XP_016866594.1:p.Glu1515Ter
XM_017011106.2:c.4414G>T	XP_016866595.1:p.Glu1472Ter
XM_017011107.2:c.4393G>T	XP_016866596.1:p.Glu1465Ter
XR_002956289.1:n.4688G>T
NM_001363725.2:c.2242G>T	NP_001350654.1:p.Glu748Ter
NM_001371656.1:c.4621G>T	NP_001358585.1:p.Glu1541Ter
NM_001374820.1:c.4621G>T	NP_001361749.1:p.Glu1541Ter
NM_001374828.1:c.4741G>T MANE Select	NP_001361757.1:p.Glu1581Ter
NM_017519.3:c.4582G>T	NP_059989.3:p.Glu1528Ter