Canonical Allele Identifier: CA366386733

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 450773
• ClinVar RCV Id: RCV000519622 ; RCV001775129
• dbSNP Id: rs1554298232
• MyVariant Identifiers: chr6:g.157431686C>T (hg19) ; chr6:g.157110552C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157110552C>T , CM000668.2:g.157110552C>T	GRCh38
NC_000006.11:g.157431686C>T , CM000668.1:g.157431686C>T	GRCh37
NC_000006.10:g.157473378C>T	NCBI36
NG_032093.1:g.337623C>T
NG_032093.2:g.337623C>T
NG_066624.1:g.339527C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2572C>T	ENSP00000055163.8:p.Gln858Ter
ENST00000414678.8:c.2492-22476C>T	ENSP00000412835.3:n.2492-22476C>T
ENST00000637015.2:c.2572C>T	ENSP00000489729.2:p.Gln858Ter
ENST00000319584.11:c.586C>T	ENSP00000313006.7:p.Gln196Ter
ENST00000346085.10:c.2611C>T	ENSP00000344546.5:p.Gln871Ter
ENST00000350026.10:c.2323C>T	ENSP00000055163.7:p.Gln775Ter
ENST00000414678.7:c.740-22476C>T	ENSP00000412835.2:n.740-22476C>T
ENST00000452544.2:n.473C>T
ENST00000493658.2:n.221C>T
ENST00000635849.1:c.73C>T	ENSP00000490948.1:p.Gln25Ter
ENST00000636930.2:c.2572C>T MANE Select	ENSP00000490491.2:p.Gln858Ter
ENST00000637003.1:c.73C>T	ENSP00000489666.1:p.Gln25Ter
ENST00000637810.1:c.73C>T	ENSP00000489636.1:p.Gln25Ter
ENST00000637904.1:c.73C>T	ENSP00000490550.1:p.Gln25Ter
ENST00000647938.1:c.2362C>T	ENSP00000498155.1:p.Gln788Ter
ENST00000674190.1:n.1321C>T
ENST00000319584.10:c.589C>T	ENSP00000313006.6:p.Gln197Ter
ENST00000346085.9:c.2362C>T	ENSP00000344546.4:p.Gln788Ter
ENST00000350026.9:c.2323C>T	ENSP00000055163.7:p.Gln775Ter
ENST00000414678.6:c.740-22476C>T	ENSP00000412835.2:n.740-22476C>T
ENST00000452544.1:n.431C>T
ENST00000493658.1:n.221C>T
NM_017519.2:c.2323C>T	NP_059989.2:p.Gln775Ter
NM_020732.3:c.2362C>T	NP_065783.3:p.Gln788Ter
XM_005267069.3:c.2323C>T	XP_005267126.2:p.Gln775Ter
XM_011535984.1:c.1273C>T	XP_011534286.1:p.Gln425Ter
XM_011535985.1:c.1273C>T	XP_011534287.1:p.Gln425Ter
XM_011535986.1:c.853C>T	XP_011534288.1:p.Gln285Ter
XM_011535987.1:c.472C>T	XP_011534289.1:p.Gln158Ter
NM_001346813.1:c.2323C>T	NP_001333742.1:p.Gln775Ter
NM_001363725.1:c.73C>T	NP_001350654.1:p.Gln25Ter
XM_011535984.2:c.2404C>T	XP_011534286.2:p.Gln802Ter
XM_017011103.2:c.2404C>T	XP_016866592.1:p.Gln802Ter
XM_017011104.1:c.2404C>T	XP_016866593.1:p.Gln802Ter
XM_017011105.2:c.2404C>T	XP_016866594.1:p.Gln802Ter
XM_017011106.2:c.2404C>T	XP_016866595.1:p.Gln802Ter
XM_017011107.2:c.2404C>T	XP_016866596.1:p.Gln802Ter
XR_002956289.1:n.2487C>T
NM_001363725.2:c.73C>T	NP_001350654.1:p.Gln25Ter
NM_001371656.1:c.2611C>T	NP_001358585.1:p.Gln871Ter
NM_001374820.1:c.2611C>T	NP_001361749.1:p.Gln871Ter
NM_001374828.1:c.2572C>T MANE Select	NP_001361757.1:p.Gln858Ter
NM_017519.3:c.2572C>T	NP_059989.3:p.Gln858Ter