Canonical Allele Identifier: CA4067183

Gene: ARID1B

Linked Data

• dbSNP Id: rs770377920
• ExAC: 6:157470066 G / A
• gnomAD v2: 6-157470066-G-A
• gnomAD v4: 6-157148932-G-A
• MyVariant Identifiers: chr6:g.157470066G>A (hg19) ; chr6:g.157148932G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148932G>A , CM000668.2:g.157148932G>A	GRCh38
NC_000006.11:g.157470066G>A , CM000668.1:g.157470066G>A	GRCh37
NC_000006.10:g.157511758G>A	NCBI36
NG_032093.1:g.376003G>A
NG_032093.2:g.376003G>A
NG_066624.1:g.377907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3070G>A	ENSP00000055163.8:p.Ala1024Thr
ENST00000414678.8:c.2980G>A	ENSP00000412835.3:p.Ala994Thr
ENST00000637015.2:c.3070G>A	ENSP00000489729.2:p.Ala1024Thr
ENST00000319584.11:c.1084G>A	ENSP00000313006.7:p.Ala362Thr
ENST00000346085.10:c.3109G>A	ENSP00000344546.5:p.Ala1037Thr
ENST00000350026.10:c.2821G>A	ENSP00000055163.7:p.Ala941Thr
ENST00000414678.7:c.1228G>A	ENSP00000412835.2:p.Ala410Thr
ENST00000452544.2:n.971G>A
ENST00000635849.1:c.391G>A	ENSP00000490948.1:p.Ala131Thr
ENST00000635957.1:c.25G>A	ENSP00000490385.1:p.Ala9Thr
ENST00000636426.1:n.204G>A
ENST00000636930.2:c.3070G>A MANE Select	ENSP00000490491.2:p.Ala1024Thr
ENST00000637015.1:c.309G>A
ENST00000637568.1:c.113G>A
ENST00000637810.1:c.571G>A	ENSP00000489636.1:p.Ala191Thr
ENST00000637904.1:c.571G>A	ENSP00000490550.1:p.Ala191Thr
ENST00000647938.1:c.2860G>A	ENSP00000498155.1:p.Ala954Thr
ENST00000674190.1:n.1819G>A
ENST00000319584.10:c.1087G>A	ENSP00000313006.6:p.Ala363Thr
ENST00000346085.9:c.2860G>A	ENSP00000344546.4:p.Ala954Thr
ENST00000350026.9:c.2821G>A	ENSP00000055163.7:p.Ala941Thr
ENST00000400790.3:c.22G>A	ENSP00000383596.3:p.Ala8Thr
ENST00000414678.6:c.1228G>A	ENSP00000412835.2:p.Ala410Thr
ENST00000452544.1:n.917G>A
ENST00000478761.3:c.143G>A
NM_017519.2:c.2821G>A	NP_059989.2:p.Ala941Thr
NM_020732.3:c.2860G>A	NP_065783.3:p.Ala954Thr
XM_005267069.3:c.2821G>A	XP_005267126.2:p.Ala941Thr
XM_011535984.1:c.1771G>A	XP_011534286.1:p.Ala591Thr
XM_011535985.1:c.1591G>A	XP_011534287.1:p.Ala531Thr
XM_011535986.1:c.1351G>A	XP_011534288.1:p.Ala451Thr
XM_011535987.1:c.970G>A	XP_011534289.1:p.Ala324Thr
XM_011535988.1:c.-20+15725G>A	XP_011534290.1:n.-20+15725G>A
NM_001346813.1:c.2821G>A	NP_001333742.1:p.Ala941Thr
NM_001363725.1:c.571G>A	NP_001350654.1:p.Ala191Thr
XM_011535984.2:c.2902G>A	XP_011534286.2:p.Ala968Thr
XM_011535988.3:c.-20+15725G>A	XP_011534290.1:n.-20+15725G>A
XM_017011103.2:c.2902G>A	XP_016866592.1:p.Ala968Thr
XM_017011104.1:c.2902G>A	XP_016866593.1:p.Ala968Thr
XM_017011105.2:c.2902G>A	XP_016866594.1:p.Ala968Thr
XM_017011106.2:c.2902G>A	XP_016866595.1:p.Ala968Thr
XM_017011107.2:c.2722G>A	XP_016866596.1:p.Ala908Thr
XR_002956289.1:n.2985G>A
NM_001363725.2:c.571G>A	NP_001350654.1:p.Ala191Thr
NM_001371656.1:c.3109G>A	NP_001358585.1:p.Ala1037Thr
NM_001374820.1:c.3109G>A	NP_001361749.1:p.Ala1037Thr
NM_001374828.1:c.3070G>A MANE Select	NP_001361757.1:p.Ala1024Thr
NM_017519.3:c.3070G>A	NP_059989.3:p.Ala1024Thr