Canonical Allele Identifier: CA452978197

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522363A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201229A>C , CM000668.2:g.157201229A>C	GRCh38
NC_000006.11:g.157522363A>C , CM000668.1:g.157522363A>C	GRCh37
NC_000006.10:g.157564055A>C	NCBI36
NG_032093.1:g.428300A>C
NG_032093.2:g.428300A>C
NG_066624.1:g.430204A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4845A>C	ENSP00000055163.8:p.Ser1615=
ENST00000414678.8:c.4914A>C	ENSP00000412835.3:p.Ser1638=
ENST00000637015.2:c.5133A>C	ENSP00000489729.2:p.Ser1711=
ENST00000346085.10:c.4884A>C	ENSP00000344546.5:p.Ser1628=
ENST00000350026.10:c.4596A>C	ENSP00000055163.7:p.Ser1532=
ENST00000414678.7:c.3162A>C	ENSP00000412835.2:p.Ser1054=
ENST00000635849.1:c.2325A>C	ENSP00000490948.1:p.Ser775=
ENST00000635957.1:c.1956A>C	ENSP00000490385.1:p.Ser652=
ENST00000636227.1:n.3467A>C
ENST00000636254.1:n.924A>C
ENST00000636930.2:c.5004A>C MANE Select	ENSP00000490491.2:p.Ser1668=
ENST00000636940.1:n.3001A>C
ENST00000637015.1:c.2372A>C
ENST00000637568.1:c.2286A>C
ENST00000637741.1:n.1670A>C
ENST00000637810.1:c.2346A>C	ENSP00000489636.1:p.Ser782=
ENST00000637904.1:c.2505A>C	ENSP00000490550.1:p.Ser835=
ENST00000647938.1:c.4635A>C	ENSP00000498155.1:p.Ser1545=
ENST00000346085.9:c.4635A>C	ENSP00000344546.4:p.Ser1545=
ENST00000350026.9:c.4596A>C	ENSP00000055163.7:p.Ser1532=
ENST00000414678.6:c.3162A>C	ENSP00000412835.2:p.Ser1054=
NM_017519.2:c.4596A>C	NP_059989.2:p.Ser1532=
NM_020732.3:c.4635A>C	NP_065783.3:p.Ser1545=
XM_005267069.3:c.4755A>C	XP_005267126.2:p.Ser1585=
XM_011535984.1:c.3834A>C	XP_011534286.1:p.Ser1278=
XM_011535985.1:c.3654A>C	XP_011534287.1:p.Ser1218=
XM_011535986.1:c.3414A>C	XP_011534288.1:p.Ser1138=
XM_011535987.1:c.3033A>C	XP_011534289.1:p.Ser1011=
XM_011535988.1:c.1896A>C	XP_011534290.1:p.Ser632=
NM_001346813.1:c.4755A>C	NP_001333742.1:p.Ser1585=
NM_001363725.1:c.2505A>C	NP_001350654.1:p.Ser835=
XM_011535984.2:c.4965A>C	XP_011534286.2:p.Ser1655=
XM_011535988.3:c.1896A>C	XP_011534290.1:p.Ser632=
XM_017011103.2:c.4866A>C	XP_016866592.1:p.Ser1622=
XM_017011104.1:c.4836A>C	XP_016866593.1:p.Ser1612=
XM_017011105.2:c.4806A>C	XP_016866594.1:p.Ser1602=
XM_017011106.2:c.4677A>C	XP_016866595.1:p.Ser1559=
XM_017011107.2:c.4656A>C	XP_016866596.1:p.Ser1552=
XR_002956289.1:n.4951A>C
NM_001363725.2:c.2505A>C	NP_001350654.1:p.Ser835=
NM_001371656.1:c.4884A>C	NP_001358585.1:p.Ser1628=
NM_001374820.1:c.4884A>C	NP_001361749.1:p.Ser1628=
NM_001374828.1:c.5004A>C MANE Select	NP_001361757.1:p.Ser1668=
NM_017519.3:c.4845A>C	NP_059989.3:p.Ser1615=