Canonical Allele Identifier: CA366241698

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522182C>A (hg19) ; chr6:g.157201048C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4664C>A	ENSP00000055163.8:p.Thr1555Lys
ENST00000414678.8:c.4733C>A	ENSP00000412835.3:p.Thr1578Lys
ENST00000637015.2:c.4952C>A	ENSP00000489729.2:p.Thr1651Lys
ENST00000346085.10:c.4703C>A	ENSP00000344546.5:p.Thr1568Lys
ENST00000350026.10:c.4415C>A	ENSP00000055163.7:p.Thr1472Lys
ENST00000414678.7:c.2981C>A	ENSP00000412835.2:p.Thr994Lys
ENST00000635849.1:c.2144C>A	ENSP00000490948.1:p.Thr715Lys
ENST00000635957.1:c.1775C>A	ENSP00000490385.1:p.Thr592Lys
ENST00000636227.1:n.3286C>A
ENST00000636254.1:n.743C>A
ENST00000636930.2:c.4823C>A MANE Select	ENSP00000490491.2:p.Thr1608Lys
ENST00000636940.1:n.2820C>A
ENST00000637015.1:c.2191C>A
ENST00000637568.1:c.2105C>A
ENST00000637741.1:n.1489C>A
ENST00000637810.1:c.2165C>A	ENSP00000489636.1:p.Thr722Lys
ENST00000637904.1:c.2324C>A	ENSP00000490550.1:p.Thr775Lys
ENST00000647938.1:c.4454C>A	ENSP00000498155.1:p.Thr1485Lys
ENST00000346085.9:c.4454C>A	ENSP00000344546.4:p.Thr1485Lys
ENST00000350026.9:c.4415C>A	ENSP00000055163.7:p.Thr1472Lys
ENST00000414678.6:c.2981C>A	ENSP00000412835.2:p.Thr994Lys
NM_017519.2:c.4415C>A	NP_059989.2:p.Thr1472Lys
NM_020732.3:c.4454C>A	NP_065783.3:p.Thr1485Lys
XM_005267069.3:c.4574C>A	XP_005267126.2:p.Thr1525Lys
XM_011535984.1:c.3653C>A	XP_011534286.1:p.Thr1218Lys
XM_011535985.1:c.3473C>A	XP_011534287.1:p.Thr1158Lys
XM_011535986.1:c.3233C>A	XP_011534288.1:p.Thr1078Lys
XM_011535987.1:c.2852C>A	XP_011534289.1:p.Thr951Lys
XM_011535988.1:c.1715C>A	XP_011534290.1:p.Thr572Lys
NM_001346813.1:c.4574C>A	NP_001333742.1:p.Thr1525Lys
NM_001363725.1:c.2324C>A	NP_001350654.1:p.Thr775Lys
XM_011535984.2:c.4784C>A	XP_011534286.2:p.Thr1595Lys
XM_011535988.3:c.1715C>A	XP_011534290.1:p.Thr572Lys
XM_017011103.2:c.4685C>A	XP_016866592.1:p.Thr1562Lys
XM_017011104.1:c.4655C>A	XP_016866593.1:p.Thr1552Lys
XM_017011105.2:c.4625C>A	XP_016866594.1:p.Thr1542Lys
XM_017011106.2:c.4496C>A	XP_016866595.1:p.Thr1499Lys
XM_017011107.2:c.4475C>A	XP_016866596.1:p.Thr1492Lys
XR_002956289.1:n.4770C>A
NM_001363725.2:c.2324C>A	NP_001350654.1:p.Thr775Lys
NM_001371656.1:c.4703C>A	NP_001358585.1:p.Thr1568Lys
NM_001374820.1:c.4703C>A	NP_001361749.1:p.Thr1568Lys
NM_001374828.1:c.4823C>A MANE Select	NP_001361757.1:p.Thr1608Lys
NM_017519.3:c.4664C>A	NP_059989.3:p.Thr1555Lys