Canonical Allele Identifier: CA4066933

Gene: ARID1B

Linked Data

• dbSNP Id: rs751192841
• ExAC: 6:157222647 C / T
• gnomAD v2: 6-157222647-C-T
• gnomAD v4: 6-156901513-C-T
• MyVariant Identifiers: chr6:g.157222647C>T (hg19) ; chr6:g.156901513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901513C>T , CM000668.2:g.156901513C>T	GRCh38
NC_000006.11:g.157222647C>T , CM000668.1:g.157222647C>T	GRCh37
NC_000006.10:g.157264339C>T	NCBI36
NG_032093.1:g.128584C>T
NG_032093.2:g.128584C>T
NG_066624.1:g.130488C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2124C>T	ENSP00000055163.8:p.Tyr708=
ENST00000414678.8:c.2124C>T	ENSP00000412835.3:p.Tyr708=
ENST00000637015.2:c.2124C>T	ENSP00000489729.2:p.Tyr708=
ENST00000319584.11:c.138C>T	ENSP00000313006.7:p.Tyr46=
ENST00000346085.10:c.2163C>T	ENSP00000344546.5:p.Tyr721=
ENST00000350026.10:c.1875C>T	ENSP00000055163.7:p.Tyr625=
ENST00000414678.7:c.372C>T	ENSP00000412835.2:p.Tyr124=
ENST00000636205.1:n.187C>T
ENST00000636748.1:c.405C>T	ENSP00000489917.1:p.Tyr135=
ENST00000636930.2:c.2124C>T MANE Select	ENSP00000490491.2:p.Tyr708=
ENST00000637532.1:c.150C>T	ENSP00000490420.1:p.Tyr50=
ENST00000638000.1:c.341C>T
ENST00000647938.1:c.1914C>T	ENSP00000498155.1:p.Tyr638=
ENST00000674190.1:n.831C>T
ENST00000674298.1:c.1864C>T
ENST00000319584.10:c.141C>T	ENSP00000313006.6:p.Tyr47=
ENST00000346085.9:c.1914C>T	ENSP00000344546.4:p.Tyr638=
ENST00000350026.9:c.1875C>T	ENSP00000055163.7:p.Tyr625=
ENST00000414678.6:c.372C>T	ENSP00000412835.2:p.Tyr124=
NM_017519.2:c.1875C>T	NP_059989.2:p.Tyr625=
NM_020732.3:c.1914C>T	NP_065783.3:p.Tyr638=
XM_005267069.3:c.1875C>T	XP_005267126.2:p.Tyr625=
XM_011535984.1:c.783C>T	XP_011534286.1:p.Tyr261=
XM_011535985.1:c.783C>T	XP_011534287.1:p.Tyr261=
XM_011535986.1:c.363C>T	XP_011534288.1:p.Tyr121=
NM_001346813.1:c.1875C>T	NP_001333742.1:p.Tyr625=
XM_011535984.2:c.1914C>T	XP_011534286.2:p.Tyr638=
XM_017011103.2:c.1914C>T	XP_016866592.1:p.Tyr638=
XM_017011104.1:c.1914C>T	XP_016866593.1:p.Tyr638=
XM_017011105.2:c.1914C>T	XP_016866594.1:p.Tyr638=
XM_017011106.2:c.1914C>T	XP_016866595.1:p.Tyr638=
XM_017011107.2:c.1914C>T	XP_016866596.1:p.Tyr638=
XR_002956289.1:n.1997C>T
NM_001371656.1:c.2163C>T	NP_001358585.1:p.Tyr721=
NM_001374820.1:c.2163C>T	NP_001361749.1:p.Tyr721=
NM_001374828.1:c.2124C>T MANE Select	NP_001361757.1:p.Tyr708=
NM_017519.3:c.2124C>T	NP_059989.3:p.Tyr708=