Canonical Allele Identifier: CA366389219

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634930
• MyVariant Identifiers: chr6:g.157470042G>A (hg19) ; chr6:g.157148908G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148908G>A , CM000668.2:g.157148908G>A	GRCh38
NC_000006.11:g.157470042G>A , CM000668.1:g.157470042G>A	GRCh37
NC_000006.10:g.157511734G>A	NCBI36
NG_032093.1:g.375979G>A
NG_032093.2:g.375979G>A
NG_066624.1:g.377883G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3046G>A	ENSP00000055163.8:p.Ala1016Thr
ENST00000414678.8:c.2956G>A	ENSP00000412835.3:p.Ala986Thr
ENST00000637015.2:c.3046G>A	ENSP00000489729.2:p.Ala1016Thr
ENST00000319584.11:c.1060G>A	ENSP00000313006.7:p.Ala354Thr
ENST00000346085.10:c.3085G>A	ENSP00000344546.5:p.Ala1029Thr
ENST00000350026.10:c.2797G>A	ENSP00000055163.7:p.Ala933Thr
ENST00000414678.7:c.1204G>A	ENSP00000412835.2:p.Ala402Thr
ENST00000452544.2:n.947G>A
ENST00000635849.1:c.367G>A	ENSP00000490948.1:p.Ala123Thr
ENST00000635957.1:c.1G>A	ENSP00000490385.1:p.Ala1Thr
ENST00000636426.1:n.180G>A
ENST00000636930.2:c.3046G>A MANE Select	ENSP00000490491.2:p.Ala1016Thr
ENST00000637015.1:c.285G>A
ENST00000637568.1:c.89G>A
ENST00000637810.1:c.547G>A	ENSP00000489636.1:p.Ala183Thr
ENST00000637904.1:c.547G>A	ENSP00000490550.1:p.Ala183Thr
ENST00000647938.1:c.2836G>A	ENSP00000498155.1:p.Ala946Thr
ENST00000674190.1:n.1795G>A
ENST00000319584.10:c.1063G>A	ENSP00000313006.6:p.Ala355Thr
ENST00000346085.9:c.2836G>A	ENSP00000344546.4:p.Ala946Thr
ENST00000350026.9:c.2797G>A	ENSP00000055163.7:p.Ala933Thr
ENST00000414678.6:c.1204G>A	ENSP00000412835.2:p.Ala402Thr
ENST00000452544.1:n.893G>A
ENST00000478761.3:c.119G>A
NM_017519.2:c.2797G>A	NP_059989.2:p.Ala933Thr
NM_020732.3:c.2836G>A	NP_065783.3:p.Ala946Thr
XM_005267069.3:c.2797G>A	XP_005267126.2:p.Ala933Thr
XM_011535984.1:c.1747G>A	XP_011534286.1:p.Ala583Thr
XM_011535985.1:c.1567G>A	XP_011534287.1:p.Ala523Thr
XM_011535986.1:c.1327G>A	XP_011534288.1:p.Ala443Thr
XM_011535987.1:c.946G>A	XP_011534289.1:p.Ala316Thr
XM_011535988.1:c.-20+15701G>A	XP_011534290.1:n.-20+15701G>A
NM_001346813.1:c.2797G>A	NP_001333742.1:p.Ala933Thr
NM_001363725.1:c.547G>A	NP_001350654.1:p.Ala183Thr
XM_011535984.2:c.2878G>A	XP_011534286.2:p.Ala960Thr
XM_011535988.3:c.-20+15701G>A	XP_011534290.1:n.-20+15701G>A
XM_017011103.2:c.2878G>A	XP_016866592.1:p.Ala960Thr
XM_017011104.1:c.2878G>A	XP_016866593.1:p.Ala960Thr
XM_017011105.2:c.2878G>A	XP_016866594.1:p.Ala960Thr
XM_017011106.2:c.2878G>A	XP_016866595.1:p.Ala960Thr
XM_017011107.2:c.2698G>A	XP_016866596.1:p.Ala900Thr
XR_002956289.1:n.2961G>A
NM_001363725.2:c.547G>A	NP_001350654.1:p.Ala183Thr
NM_001371656.1:c.3085G>A	NP_001358585.1:p.Ala1029Thr
NM_001374820.1:c.3085G>A	NP_001361749.1:p.Ala1029Thr
NM_001374828.1:c.3046G>A MANE Select	NP_001361757.1:p.Ala1016Thr
NM_017519.3:c.3046G>A	NP_059989.3:p.Ala1016Thr