Canonical Allele Identifier: CA366384047

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 520639
• ClinVar RCV Id: RCV000624037 ; RCV000679918 ; RCV001533085
• dbSNP Id: rs1554256703
• MyVariant Identifiers: chr6:g.157150436C>T (hg19) ; chr6:g.156829302C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829302C>T , CM000668.2:g.156829302C>T	GRCh38
NC_000006.11:g.157150436C>T , CM000668.1:g.157150436C>T	GRCh37
NC_000006.10:g.157192128C>T	NCBI36
NG_032093.1:g.56373C>T
NG_032093.2:g.56373C>T
NG_066624.1:g.58277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.1867C>T	ENSP00000055163.8:p.Gln623Ter
ENST00000414678.8:c.1867C>T	ENSP00000412835.3:p.Gln623Ter
ENST00000637015.2:c.1867C>T	ENSP00000489729.2:p.Gln623Ter
ENST00000346085.10:c.1867C>T	ENSP00000344546.5:p.Gln623Ter
ENST00000350026.10:c.1618C>T	ENSP00000055163.7:p.Gln540Ter
ENST00000414678.7:c.115C>T	ENSP00000412835.2:p.Gln39Ter
ENST00000494260.2:c.148C>T	ENSP00000490094.1:p.Gln50Ter
ENST00000636607.1:c.130C>T	ENSP00000490050.1:p.Gln44Ter
ENST00000636748.1:c.148C>T	ENSP00000489917.1:p.Gln50Ter
ENST00000636930.2:c.1867C>T MANE Select	ENSP00000490491.2:p.Gln623Ter
ENST00000637910.1:n.148C>T
ENST00000638000.1:c.84C>T
ENST00000647938.1:c.1618C>T	ENSP00000498155.1:p.Gln540Ter
ENST00000674190.1:n.574C>T
ENST00000674298.1:c.1607C>T
ENST00000346085.9:c.1618C>T	ENSP00000344546.4:p.Gln540Ter
ENST00000350026.9:c.1618C>T	ENSP00000055163.7:p.Gln540Ter
ENST00000414678.6:c.115C>T	ENSP00000412835.2:p.Gln39Ter
ENST00000494260.1:n.76C>T
NM_017519.2:c.1618C>T	NP_059989.2:p.Gln540Ter
NM_020732.3:c.1618C>T	NP_065783.3:p.Gln540Ter
XM_005267069.3:c.1618C>T	XP_005267126.2:p.Gln540Ter
XM_011535984.1:c.487C>T	XP_011534286.1:p.Gln163Ter
XM_011535985.1:c.487C>T	XP_011534287.1:p.Gln163Ter
XM_011535986.1:c.67C>T	XP_011534288.1:p.Gln23Ter
NM_001346813.1:c.1618C>T	NP_001333742.1:p.Gln540Ter
XM_011535984.2:c.1618C>T	XP_011534286.2:p.Gln540Ter
XM_017011103.2:c.1618C>T	XP_016866592.1:p.Gln540Ter
XM_017011104.1:c.1618C>T	XP_016866593.1:p.Gln540Ter
XM_017011105.2:c.1618C>T	XP_016866594.1:p.Gln540Ter
XM_017011106.2:c.1618C>T	XP_016866595.1:p.Gln540Ter
XM_017011107.2:c.1618C>T	XP_016866596.1:p.Gln540Ter
XR_002956289.1:n.1701C>T
NM_001371656.1:c.1867C>T	NP_001358585.1:p.Gln623Ter
NM_001374820.1:c.1867C>T	NP_001361749.1:p.Gln623Ter
NM_001374828.1:c.1867C>T MANE Select	NP_001361757.1:p.Gln623Ter
NM_017519.3:c.1867C>T	NP_059989.3:p.Gln623Ter