Canonical Allele Identifier: CA16609413

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 397537
• ClinVar RCV Id: RCV000449505
• dbSNP Id: rs1060499668
• MyVariant Identifiers: chr6:g.157150553C>T (hg19) ; chr6:g.156829419C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829419C>T , CM000668.2:g.156829419C>T	GRCh38
NC_000006.11:g.157150553C>T , CM000668.1:g.157150553C>T	GRCh37
NC_000006.10:g.157192245C>T	NCBI36
NG_032093.1:g.56490C>T
NG_032093.2:g.56490C>T
NG_066624.1:g.58394C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.1984C>T	ENSP00000055163.8:p.Gln662Ter
ENST00000414678.8:c.1984C>T	ENSP00000412835.3:p.Gln662Ter
ENST00000637015.2:c.1984C>T	ENSP00000489729.2:p.Gln662Ter
ENST00000346085.10:c.1984C>T	ENSP00000344546.5:p.Gln662Ter
ENST00000350026.10:c.1735C>T	ENSP00000055163.7:p.Gln579Ter
ENST00000414678.7:c.232C>T	ENSP00000412835.2:p.Gln78Ter
ENST00000494260.2:c.265C>T	ENSP00000490094.1:p.Gln89Ter
ENST00000636205.1:n.47C>T
ENST00000636607.1:c.247C>T	ENSP00000490050.1:p.Gln83Ter
ENST00000636748.1:c.265C>T	ENSP00000489917.1:p.Gln89Ter
ENST00000636930.2:c.1984C>T MANE Select	ENSP00000490491.2:p.Gln662Ter
ENST00000637532.1:c.10C>T	ENSP00000490420.1:p.Gln4Ter
ENST00000637910.1:n.265C>T
ENST00000638000.1:c.201C>T
ENST00000647938.1:c.1735C>T	ENSP00000498155.1:p.Gln579Ter
ENST00000674190.1:n.691C>T
ENST00000674298.1:c.1724C>T
ENST00000346085.9:c.1735C>T	ENSP00000344546.4:p.Gln579Ter
ENST00000350026.9:c.1735C>T	ENSP00000055163.7:p.Gln579Ter
ENST00000414678.6:c.232C>T	ENSP00000412835.2:p.Gln78Ter
ENST00000494260.1:n.193C>T
NM_017519.2:c.1735C>T	NP_059989.2:p.Gln579Ter
NM_020732.3:c.1735C>T	NP_065783.3:p.Gln579Ter
XM_005267069.3:c.1735C>T	XP_005267126.2:p.Gln579Ter
XM_011535984.1:c.604C>T	XP_011534286.1:p.Gln202Ter
XM_011535985.1:c.604C>T	XP_011534287.1:p.Gln202Ter
XM_011535986.1:c.184C>T	XP_011534288.1:p.Gln62Ter
NM_001346813.1:c.1735C>T	NP_001333742.1:p.Gln579Ter
XM_011535984.2:c.1735C>T	XP_011534286.2:p.Gln579Ter
XM_017011103.2:c.1735C>T	XP_016866592.1:p.Gln579Ter
XM_017011104.1:c.1735C>T	XP_016866593.1:p.Gln579Ter
XM_017011105.2:c.1735C>T	XP_016866594.1:p.Gln579Ter
XM_017011106.2:c.1735C>T	XP_016866595.1:p.Gln579Ter
XM_017011107.2:c.1735C>T	XP_016866596.1:p.Gln579Ter
XR_002956289.1:n.1818C>T
NM_001371656.1:c.1984C>T	NP_001358585.1:p.Gln662Ter
NM_001374820.1:c.1984C>T	NP_001361749.1:p.Gln662Ter
NM_001374828.1:c.1984C>T MANE Select	NP_001361757.1:p.Gln662Ter
NM_017519.3:c.1984C>T	NP_059989.3:p.Gln662Ter