Canonical Allele Identifier: CA366389221

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470042G>T (hg19) ; chr6:g.157148908G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3046G>T	ENSP00000055163.8:p.Ala1016Ser
ENST00000414678.8:c.2956G>T	ENSP00000412835.3:p.Ala986Ser
ENST00000637015.2:c.3046G>T	ENSP00000489729.2:p.Ala1016Ser
ENST00000319584.11:c.1060G>T	ENSP00000313006.7:p.Ala354Ser
ENST00000346085.10:c.3085G>T	ENSP00000344546.5:p.Ala1029Ser
ENST00000350026.10:c.2797G>T	ENSP00000055163.7:p.Ala933Ser
ENST00000414678.7:c.1204G>T	ENSP00000412835.2:p.Ala402Ser
ENST00000452544.2:n.947G>T
ENST00000635849.1:c.367G>T	ENSP00000490948.1:p.Ala123Ser
ENST00000635957.1:c.1G>T	ENSP00000490385.1:p.Ala1Ser
ENST00000636426.1:n.180G>T
ENST00000636930.2:c.3046G>T MANE Select	ENSP00000490491.2:p.Ala1016Ser
ENST00000637015.1:c.285G>T
ENST00000637568.1:c.89G>T
ENST00000637810.1:c.547G>T	ENSP00000489636.1:p.Ala183Ser
ENST00000637904.1:c.547G>T	ENSP00000490550.1:p.Ala183Ser
ENST00000647938.1:c.2836G>T	ENSP00000498155.1:p.Ala946Ser
ENST00000674190.1:n.1795G>T
ENST00000319584.10:c.1063G>T	ENSP00000313006.6:p.Ala355Ser
ENST00000346085.9:c.2836G>T	ENSP00000344546.4:p.Ala946Ser
ENST00000350026.9:c.2797G>T	ENSP00000055163.7:p.Ala933Ser
ENST00000414678.6:c.1204G>T	ENSP00000412835.2:p.Ala402Ser
ENST00000452544.1:n.893G>T
ENST00000478761.3:c.119G>T
NM_017519.2:c.2797G>T	NP_059989.2:p.Ala933Ser
NM_020732.3:c.2836G>T	NP_065783.3:p.Ala946Ser
XM_005267069.3:c.2797G>T	XP_005267126.2:p.Ala933Ser
XM_011535984.1:c.1747G>T	XP_011534286.1:p.Ala583Ser
XM_011535985.1:c.1567G>T	XP_011534287.1:p.Ala523Ser
XM_011535986.1:c.1327G>T	XP_011534288.1:p.Ala443Ser
XM_011535987.1:c.946G>T	XP_011534289.1:p.Ala316Ser
XM_011535988.1:c.-20+15701G>T	XP_011534290.1:n.-20+15701G>T
NM_001346813.1:c.2797G>T	NP_001333742.1:p.Ala933Ser
NM_001363725.1:c.547G>T	NP_001350654.1:p.Ala183Ser
XM_011535984.2:c.2878G>T	XP_011534286.2:p.Ala960Ser
XM_011535988.3:c.-20+15701G>T	XP_011534290.1:n.-20+15701G>T
XM_017011103.2:c.2878G>T	XP_016866592.1:p.Ala960Ser
XM_017011104.1:c.2878G>T	XP_016866593.1:p.Ala960Ser
XM_017011105.2:c.2878G>T	XP_016866594.1:p.Ala960Ser
XM_017011106.2:c.2878G>T	XP_016866595.1:p.Ala960Ser
XM_017011107.2:c.2698G>T	XP_016866596.1:p.Ala900Ser
XR_002956289.1:n.2961G>T
NM_001363725.2:c.547G>T	NP_001350654.1:p.Ala183Ser
NM_001371656.1:c.3085G>T	NP_001358585.1:p.Ala1029Ser
NM_001374820.1:c.3085G>T	NP_001361749.1:p.Ala1029Ser
NM_001374828.1:c.3046G>T MANE Select	NP_001361757.1:p.Ala1016Ser
NM_017519.3:c.3046G>T	NP_059989.3:p.Ala1016Ser