Canonical Allele Identifier: CA4066931

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2123A>C	ENSP00000055163.8:p.Tyr708Ser
ENST00000414678.8:c.2123A>C	ENSP00000412835.3:p.Tyr708Ser
ENST00000637015.2:c.2123A>C	ENSP00000489729.2:p.Tyr708Ser
ENST00000319584.11:c.137A>C	ENSP00000313006.7:p.Tyr46Ser
ENST00000346085.10:c.2162A>C	ENSP00000344546.5:p.Tyr721Ser
ENST00000350026.10:c.1874A>C	ENSP00000055163.7:p.Tyr625Ser
ENST00000414678.7:c.371A>C	ENSP00000412835.2:p.Tyr124Ser
ENST00000636205.1:n.186A>C
ENST00000636748.1:c.404A>C	ENSP00000489917.1:p.Tyr135Ser
ENST00000636930.2:c.2123A>C MANE Select	ENSP00000490491.2:p.Tyr708Ser
ENST00000637532.1:c.149A>C	ENSP00000490420.1:p.Tyr50Ser
ENST00000638000.1:c.340A>C
ENST00000647938.1:c.1913A>C	ENSP00000498155.1:p.Tyr638Ser
ENST00000674190.1:n.830A>C
ENST00000674298.1:c.1863A>C
ENST00000319584.10:c.140A>C	ENSP00000313006.6:p.Tyr47Ser
ENST00000346085.9:c.1913A>C	ENSP00000344546.4:p.Tyr638Ser
ENST00000350026.9:c.1874A>C	ENSP00000055163.7:p.Tyr625Ser
ENST00000414678.6:c.371A>C	ENSP00000412835.2:p.Tyr124Ser
NM_017519.2:c.1874A>C	NP_059989.2:p.Tyr625Ser
NM_020732.3:c.1913A>C	NP_065783.3:p.Tyr638Ser
XM_005267069.3:c.1874A>C	XP_005267126.2:p.Tyr625Ser
XM_011535984.1:c.782A>C	XP_011534286.1:p.Tyr261Ser
XM_011535985.1:c.782A>C	XP_011534287.1:p.Tyr261Ser
XM_011535986.1:c.362A>C	XP_011534288.1:p.Tyr121Ser
NM_001346813.1:c.1874A>C	NP_001333742.1:p.Tyr625Ser
XM_011535984.2:c.1913A>C	XP_011534286.2:p.Tyr638Ser
XM_017011103.2:c.1913A>C	XP_016866592.1:p.Tyr638Ser
XM_017011104.1:c.1913A>C	XP_016866593.1:p.Tyr638Ser
XM_017011105.2:c.1913A>C	XP_016866594.1:p.Tyr638Ser
XM_017011106.2:c.1913A>C	XP_016866595.1:p.Tyr638Ser
XM_017011107.2:c.1913A>C	XP_016866596.1:p.Tyr638Ser
XR_002956289.1:n.1996A>C
NM_001371656.1:c.2162A>C	NP_001358585.1:p.Tyr721Ser
NM_001374820.1:c.2162A>C	NP_001361749.1:p.Tyr721Ser
NM_001374828.1:c.2123A>C MANE Select	NP_001361757.1:p.Tyr708Ser
NM_017519.3:c.2123A>C	NP_059989.3:p.Tyr708Ser