Canonical Allele Identifier: CA452989846

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157405912G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084778G>T , CM000668.2:g.157084778G>T	GRCh38
NC_000006.11:g.157405912G>T , CM000668.1:g.157405912G>T	GRCh37
NC_000006.10:g.157447604G>T	NCBI36
NG_032093.1:g.311849G>T
NG_032093.2:g.311849G>T
NG_066624.1:g.313753G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2364G>T	ENSP00000055163.8:p.Ser788=
ENST00000414678.8:c.2364G>T	ENSP00000412835.3:p.Ser788=
ENST00000637015.2:c.2364G>T	ENSP00000489729.2:p.Ser788=
ENST00000319584.11:c.378G>T	ENSP00000313006.7:p.Ser126=
ENST00000346085.10:c.2403G>T	ENSP00000344546.5:p.Ser801=
ENST00000350026.10:c.2115G>T	ENSP00000055163.7:p.Ser705=
ENST00000414678.7:c.612G>T	ENSP00000412835.2:p.Ser204=
ENST00000452544.2:n.265G>T
ENST00000493658.2:n.13G>T
ENST00000635849.1:c.-136G>T	ENSP00000490948.1:n.-136G>T
ENST00000636930.2:c.2364G>T MANE Select	ENSP00000490491.2:p.Ser788=
ENST00000637003.1:c.-136G>T	ENSP00000489666.1:n.-136G>T
ENST00000637810.1:c.-136G>T	ENSP00000489636.1:n.-136G>T
ENST00000637904.1:c.-136G>T	ENSP00000490550.1:n.-136G>T
ENST00000647938.1:c.2154G>T	ENSP00000498155.1:p.Ser718=
ENST00000674190.1:n.1113G>T
ENST00000319584.10:c.381G>T	ENSP00000313006.6:p.Ser127=
ENST00000346085.9:c.2154G>T	ENSP00000344546.4:p.Ser718=
ENST00000350026.9:c.2115G>T	ENSP00000055163.7:p.Ser705=
ENST00000414678.6:c.612G>T	ENSP00000412835.2:p.Ser204=
ENST00000452544.1:n.223G>T
ENST00000493658.1:n.13G>T
NM_017519.2:c.2115G>T	NP_059989.2:p.Ser705=
NM_020732.3:c.2154G>T	NP_065783.3:p.Ser718=
XM_005267069.3:c.2115G>T	XP_005267126.2:p.Ser705=
XM_011535984.1:c.1065G>T	XP_011534286.1:p.Ser355=
XM_011535985.1:c.1065G>T	XP_011534287.1:p.Ser355=
XM_011535986.1:c.645G>T	XP_011534288.1:p.Ser215=
XM_011535987.1:c.264G>T	XP_011534289.1:p.Ser88=
NM_001346813.1:c.2115G>T	NP_001333742.1:p.Ser705=
NM_001363725.1:c.-136G>T	NP_001350654.1:n.-136G>T
XM_011535984.2:c.2196G>T	XP_011534286.2:p.Ser732=
XM_017011103.2:c.2196G>T	XP_016866592.1:p.Ser732=
XM_017011104.1:c.2196G>T	XP_016866593.1:p.Ser732=
XM_017011105.2:c.2196G>T	XP_016866594.1:p.Ser732=
XM_017011106.2:c.2196G>T	XP_016866595.1:p.Ser732=
XM_017011107.2:c.2196G>T	XP_016866596.1:p.Ser732=
XR_002956289.1:n.2279G>T
NM_001363725.2:c.-136G>T	NP_001350654.1:n.-136G>T
NM_001371656.1:c.2403G>T	NP_001358585.1:p.Ser801=
NM_001374820.1:c.2403G>T	NP_001361749.1:p.Ser801=
NM_001374828.1:c.2364G>T MANE Select	NP_001361757.1:p.Ser788=
NM_017519.3:c.2364G>T	NP_059989.3:p.Ser788=