Canonical Allele Identifier: CA366241722

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522187G>A (hg19) ; chr6:g.157201053G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201053G>A , CM000668.2:g.157201053G>A	GRCh38
NC_000006.11:g.157522187G>A , CM000668.1:g.157522187G>A	GRCh37
NC_000006.10:g.157563879G>A	NCBI36
NG_032093.1:g.428124G>A
NG_032093.2:g.428124G>A
NG_066624.1:g.430028G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4669G>A	ENSP00000055163.8:p.Ala1557Thr
ENST00000414678.8:c.4738G>A	ENSP00000412835.3:p.Ala1580Thr
ENST00000637015.2:c.4957G>A	ENSP00000489729.2:p.Ala1653Thr
ENST00000346085.10:c.4708G>A	ENSP00000344546.5:p.Ala1570Thr
ENST00000350026.10:c.4420G>A	ENSP00000055163.7:p.Ala1474Thr
ENST00000414678.7:c.2986G>A	ENSP00000412835.2:p.Ala996Thr
ENST00000635849.1:c.2149G>A	ENSP00000490948.1:p.Ala717Thr
ENST00000635957.1:c.1780G>A	ENSP00000490385.1:p.Ala594Thr
ENST00000636227.1:n.3291G>A
ENST00000636254.1:n.748G>A
ENST00000636930.2:c.4828G>A MANE Select	ENSP00000490491.2:p.Ala1610Thr
ENST00000636940.1:n.2825G>A
ENST00000637015.1:c.2196G>A
ENST00000637568.1:c.2110G>A
ENST00000637741.1:n.1494G>A
ENST00000637810.1:c.2170G>A	ENSP00000489636.1:p.Ala724Thr
ENST00000637904.1:c.2329G>A	ENSP00000490550.1:p.Ala777Thr
ENST00000647938.1:c.4459G>A	ENSP00000498155.1:p.Ala1487Thr
ENST00000346085.9:c.4459G>A	ENSP00000344546.4:p.Ala1487Thr
ENST00000350026.9:c.4420G>A	ENSP00000055163.7:p.Ala1474Thr
ENST00000414678.6:c.2986G>A	ENSP00000412835.2:p.Ala996Thr
NM_017519.2:c.4420G>A	NP_059989.2:p.Ala1474Thr
NM_020732.3:c.4459G>A	NP_065783.3:p.Ala1487Thr
XM_005267069.3:c.4579G>A	XP_005267126.2:p.Ala1527Thr
XM_011535984.1:c.3658G>A	XP_011534286.1:p.Ala1220Thr
XM_011535985.1:c.3478G>A	XP_011534287.1:p.Ala1160Thr
XM_011535986.1:c.3238G>A	XP_011534288.1:p.Ala1080Thr
XM_011535987.1:c.2857G>A	XP_011534289.1:p.Ala953Thr
XM_011535988.1:c.1720G>A	XP_011534290.1:p.Ala574Thr
NM_001346813.1:c.4579G>A	NP_001333742.1:p.Ala1527Thr
NM_001363725.1:c.2329G>A	NP_001350654.1:p.Ala777Thr
XM_011535984.2:c.4789G>A	XP_011534286.2:p.Ala1597Thr
XM_011535988.3:c.1720G>A	XP_011534290.1:p.Ala574Thr
XM_017011103.2:c.4690G>A	XP_016866592.1:p.Ala1564Thr
XM_017011104.1:c.4660G>A	XP_016866593.1:p.Ala1554Thr
XM_017011105.2:c.4630G>A	XP_016866594.1:p.Ala1544Thr
XM_017011106.2:c.4501G>A	XP_016866595.1:p.Ala1501Thr
XM_017011107.2:c.4480G>A	XP_016866596.1:p.Ala1494Thr
XR_002956289.1:n.4775G>A
NM_001363725.2:c.2329G>A	NP_001350654.1:p.Ala777Thr
NM_001371656.1:c.4708G>A	NP_001358585.1:p.Ala1570Thr
NM_001374820.1:c.4708G>A	NP_001361749.1:p.Ala1570Thr
NM_001374828.1:c.4828G>A MANE Select	NP_001361757.1:p.Ala1610Thr
NM_017519.3:c.4669G>A	NP_059989.3:p.Ala1557Thr