Canonical Allele Identifier: CA366241700

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374163
• MyVariant Identifiers: chr6:g.157522182C>T (hg19) ; chr6:g.157201048C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201048C>T , CM000668.2:g.157201048C>T	GRCh38
NC_000006.11:g.157522182C>T , CM000668.1:g.157522182C>T	GRCh37
NC_000006.10:g.157563874C>T	NCBI36
NG_032093.1:g.428119C>T
NG_032093.2:g.428119C>T
NG_066624.1:g.430023C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4664C>T	ENSP00000055163.8:p.Thr1555Ile
ENST00000414678.8:c.4733C>T	ENSP00000412835.3:p.Thr1578Ile
ENST00000637015.2:c.4952C>T	ENSP00000489729.2:p.Thr1651Ile
ENST00000346085.10:c.4703C>T	ENSP00000344546.5:p.Thr1568Ile
ENST00000350026.10:c.4415C>T	ENSP00000055163.7:p.Thr1472Ile
ENST00000414678.7:c.2981C>T	ENSP00000412835.2:p.Thr994Ile
ENST00000635849.1:c.2144C>T	ENSP00000490948.1:p.Thr715Ile
ENST00000635957.1:c.1775C>T	ENSP00000490385.1:p.Thr592Ile
ENST00000636227.1:n.3286C>T
ENST00000636254.1:n.743C>T
ENST00000636930.2:c.4823C>T MANE Select	ENSP00000490491.2:p.Thr1608Ile
ENST00000636940.1:n.2820C>T
ENST00000637015.1:c.2191C>T
ENST00000637568.1:c.2105C>T
ENST00000637741.1:n.1489C>T
ENST00000637810.1:c.2165C>T	ENSP00000489636.1:p.Thr722Ile
ENST00000637904.1:c.2324C>T	ENSP00000490550.1:p.Thr775Ile
ENST00000647938.1:c.4454C>T	ENSP00000498155.1:p.Thr1485Ile
ENST00000346085.9:c.4454C>T	ENSP00000344546.4:p.Thr1485Ile
ENST00000350026.9:c.4415C>T	ENSP00000055163.7:p.Thr1472Ile
ENST00000414678.6:c.2981C>T	ENSP00000412835.2:p.Thr994Ile
NM_017519.2:c.4415C>T	NP_059989.2:p.Thr1472Ile
NM_020732.3:c.4454C>T	NP_065783.3:p.Thr1485Ile
XM_005267069.3:c.4574C>T	XP_005267126.2:p.Thr1525Ile
XM_011535984.1:c.3653C>T	XP_011534286.1:p.Thr1218Ile
XM_011535985.1:c.3473C>T	XP_011534287.1:p.Thr1158Ile
XM_011535986.1:c.3233C>T	XP_011534288.1:p.Thr1078Ile
XM_011535987.1:c.2852C>T	XP_011534289.1:p.Thr951Ile
XM_011535988.1:c.1715C>T	XP_011534290.1:p.Thr572Ile
NM_001346813.1:c.4574C>T	NP_001333742.1:p.Thr1525Ile
NM_001363725.1:c.2324C>T	NP_001350654.1:p.Thr775Ile
XM_011535984.2:c.4784C>T	XP_011534286.2:p.Thr1595Ile
XM_011535988.3:c.1715C>T	XP_011534290.1:p.Thr572Ile
XM_017011103.2:c.4685C>T	XP_016866592.1:p.Thr1562Ile
XM_017011104.1:c.4655C>T	XP_016866593.1:p.Thr1552Ile
XM_017011105.2:c.4625C>T	XP_016866594.1:p.Thr1542Ile
XM_017011106.2:c.4496C>T	XP_016866595.1:p.Thr1499Ile
XM_017011107.2:c.4475C>T	XP_016866596.1:p.Thr1492Ile
XR_002956289.1:n.4770C>T
NM_001363725.2:c.2324C>T	NP_001350654.1:p.Thr775Ile
NM_001371656.1:c.4703C>T	NP_001358585.1:p.Thr1568Ile
NM_001374820.1:c.4703C>T	NP_001361749.1:p.Thr1568Ile
NM_001374828.1:c.4823C>T MANE Select	NP_001361757.1:p.Thr1608Ile
NM_017519.3:c.4664C>T	NP_059989.3:p.Thr1555Ile