Canonical Allele Identifier: CA366242272

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522355C>A (hg19) ; chr6:g.157201221C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201221C>A , CM000668.2:g.157201221C>A	GRCh38
NC_000006.11:g.157522355C>A , CM000668.1:g.157522355C>A	GRCh37
NC_000006.10:g.157564047C>A	NCBI36
NG_032093.1:g.428292C>A
NG_032093.2:g.428292C>A
NG_066624.1:g.430196C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4837C>A	ENSP00000055163.8:p.Pro1613Thr
ENST00000414678.8:c.4906C>A	ENSP00000412835.3:p.Pro1636Thr
ENST00000637015.2:c.5125C>A	ENSP00000489729.2:p.Pro1709Thr
ENST00000346085.10:c.4876C>A	ENSP00000344546.5:p.Pro1626Thr
ENST00000350026.10:c.4588C>A	ENSP00000055163.7:p.Pro1530Thr
ENST00000414678.7:c.3154C>A	ENSP00000412835.2:p.Pro1052Thr
ENST00000635849.1:c.2317C>A	ENSP00000490948.1:p.Pro773Thr
ENST00000635957.1:c.1948C>A	ENSP00000490385.1:p.Pro650Thr
ENST00000636227.1:n.3459C>A
ENST00000636254.1:n.916C>A
ENST00000636930.2:c.4996C>A MANE Select	ENSP00000490491.2:p.Pro1666Thr
ENST00000636940.1:n.2993C>A
ENST00000637015.1:c.2364C>A
ENST00000637568.1:c.2278C>A
ENST00000637741.1:n.1662C>A
ENST00000637810.1:c.2338C>A	ENSP00000489636.1:p.Pro780Thr
ENST00000637904.1:c.2497C>A	ENSP00000490550.1:p.Pro833Thr
ENST00000647938.1:c.4627C>A	ENSP00000498155.1:p.Pro1543Thr
ENST00000346085.9:c.4627C>A	ENSP00000344546.4:p.Pro1543Thr
ENST00000350026.9:c.4588C>A	ENSP00000055163.7:p.Pro1530Thr
ENST00000414678.6:c.3154C>A	ENSP00000412835.2:p.Pro1052Thr
NM_017519.2:c.4588C>A	NP_059989.2:p.Pro1530Thr
NM_020732.3:c.4627C>A	NP_065783.3:p.Pro1543Thr
XM_005267069.3:c.4747C>A	XP_005267126.2:p.Pro1583Thr
XM_011535984.1:c.3826C>A	XP_011534286.1:p.Pro1276Thr
XM_011535985.1:c.3646C>A	XP_011534287.1:p.Pro1216Thr
XM_011535986.1:c.3406C>A	XP_011534288.1:p.Pro1136Thr
XM_011535987.1:c.3025C>A	XP_011534289.1:p.Pro1009Thr
XM_011535988.1:c.1888C>A	XP_011534290.1:p.Pro630Thr
NM_001346813.1:c.4747C>A	NP_001333742.1:p.Pro1583Thr
NM_001363725.1:c.2497C>A	NP_001350654.1:p.Pro833Thr
XM_011535984.2:c.4957C>A	XP_011534286.2:p.Pro1653Thr
XM_011535988.3:c.1888C>A	XP_011534290.1:p.Pro630Thr
XM_017011103.2:c.4858C>A	XP_016866592.1:p.Pro1620Thr
XM_017011104.1:c.4828C>A	XP_016866593.1:p.Pro1610Thr
XM_017011105.2:c.4798C>A	XP_016866594.1:p.Pro1600Thr
XM_017011106.2:c.4669C>A	XP_016866595.1:p.Pro1557Thr
XM_017011107.2:c.4648C>A	XP_016866596.1:p.Pro1550Thr
XR_002956289.1:n.4943C>A
NM_001363725.2:c.2497C>A	NP_001350654.1:p.Pro833Thr
NM_001371656.1:c.4876C>A	NP_001358585.1:p.Pro1626Thr
NM_001374820.1:c.4876C>A	NP_001361749.1:p.Pro1626Thr
NM_001374828.1:c.4996C>A MANE Select	NP_001361757.1:p.Pro1666Thr
NM_017519.3:c.4837C>A	NP_059989.3:p.Pro1613Thr