Canonical Allele Identifier: CA4066932

Gene: ARID1B

Linked Data

• dbSNP Id: rs759934770
• ExAC: 6:157222646 A / T
• gnomAD v2: 6-157222646-A-T
• gnomAD v4: 6-156901512-A-T
• MyVariant Identifiers: chr6:g.157222646A>T (hg19) ; chr6:g.156901512A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901512A>T , CM000668.2:g.156901512A>T	GRCh38
NC_000006.11:g.157222646A>T , CM000668.1:g.157222646A>T	GRCh37
NC_000006.10:g.157264338A>T	NCBI36
NG_032093.1:g.128583A>T
NG_032093.2:g.128583A>T
NG_066624.1:g.130487A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2123A>T	ENSP00000055163.8:p.Tyr708Phe
ENST00000414678.8:c.2123A>T	ENSP00000412835.3:p.Tyr708Phe
ENST00000637015.2:c.2123A>T	ENSP00000489729.2:p.Tyr708Phe
ENST00000319584.11:c.137A>T	ENSP00000313006.7:p.Tyr46Phe
ENST00000346085.10:c.2162A>T	ENSP00000344546.5:p.Tyr721Phe
ENST00000350026.10:c.1874A>T	ENSP00000055163.7:p.Tyr625Phe
ENST00000414678.7:c.371A>T	ENSP00000412835.2:p.Tyr124Phe
ENST00000636205.1:n.186A>T
ENST00000636748.1:c.404A>T	ENSP00000489917.1:p.Tyr135Phe
ENST00000636930.2:c.2123A>T MANE Select	ENSP00000490491.2:p.Tyr708Phe
ENST00000637532.1:c.149A>T	ENSP00000490420.1:p.Tyr50Phe
ENST00000638000.1:c.340A>T
ENST00000647938.1:c.1913A>T	ENSP00000498155.1:p.Tyr638Phe
ENST00000674190.1:n.830A>T
ENST00000674298.1:c.1863A>T
ENST00000319584.10:c.140A>T	ENSP00000313006.6:p.Tyr47Phe
ENST00000346085.9:c.1913A>T	ENSP00000344546.4:p.Tyr638Phe
ENST00000350026.9:c.1874A>T	ENSP00000055163.7:p.Tyr625Phe
ENST00000414678.6:c.371A>T	ENSP00000412835.2:p.Tyr124Phe
NM_017519.2:c.1874A>T	NP_059989.2:p.Tyr625Phe
NM_020732.3:c.1913A>T	NP_065783.3:p.Tyr638Phe
XM_005267069.3:c.1874A>T	XP_005267126.2:p.Tyr625Phe
XM_011535984.1:c.782A>T	XP_011534286.1:p.Tyr261Phe
XM_011535985.1:c.782A>T	XP_011534287.1:p.Tyr261Phe
XM_011535986.1:c.362A>T	XP_011534288.1:p.Tyr121Phe
NM_001346813.1:c.1874A>T	NP_001333742.1:p.Tyr625Phe
XM_011535984.2:c.1913A>T	XP_011534286.2:p.Tyr638Phe
XM_017011103.2:c.1913A>T	XP_016866592.1:p.Tyr638Phe
XM_017011104.1:c.1913A>T	XP_016866593.1:p.Tyr638Phe
XM_017011105.2:c.1913A>T	XP_016866594.1:p.Tyr638Phe
XM_017011106.2:c.1913A>T	XP_016866595.1:p.Tyr638Phe
XM_017011107.2:c.1913A>T	XP_016866596.1:p.Tyr638Phe
XR_002956289.1:n.1996A>T
NM_001371656.1:c.2162A>T	NP_001358585.1:p.Tyr721Phe
NM_001374820.1:c.2162A>T	NP_001361749.1:p.Tyr721Phe
NM_001374828.1:c.2123A>T MANE Select	NP_001361757.1:p.Tyr708Phe
NM_017519.3:c.2123A>T	NP_059989.3:p.Tyr708Phe