Canonical Allele Identifier: CA452978428

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522222T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201088T>C , CM000668.2:g.157201088T>C	GRCh38
NC_000006.11:g.157522222T>C , CM000668.1:g.157522222T>C	GRCh37
NC_000006.10:g.157563914T>C	NCBI36
NG_032093.1:g.428159T>C
NG_032093.2:g.428159T>C
NG_066624.1:g.430063T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4704T>C	ENSP00000055163.8:p.Asp1568=
ENST00000414678.8:c.4773T>C	ENSP00000412835.3:p.Asp1591=
ENST00000637015.2:c.4992T>C	ENSP00000489729.2:p.Asp1664=
ENST00000346085.10:c.4743T>C	ENSP00000344546.5:p.Asp1581=
ENST00000350026.10:c.4455T>C	ENSP00000055163.7:p.Asp1485=
ENST00000414678.7:c.3021T>C	ENSP00000412835.2:p.Asp1007=
ENST00000635849.1:c.2184T>C	ENSP00000490948.1:p.Asp728=
ENST00000635957.1:c.1815T>C	ENSP00000490385.1:p.Asp605=
ENST00000636227.1:n.3326T>C
ENST00000636254.1:n.783T>C
ENST00000636930.2:c.4863T>C MANE Select	ENSP00000490491.2:p.Asp1621=
ENST00000636940.1:n.2860T>C
ENST00000637015.1:c.2231T>C
ENST00000637568.1:c.2145T>C
ENST00000637741.1:n.1529T>C
ENST00000637810.1:c.2205T>C	ENSP00000489636.1:p.Asp735=
ENST00000637904.1:c.2364T>C	ENSP00000490550.1:p.Asp788=
ENST00000647938.1:c.4494T>C	ENSP00000498155.1:p.Asp1498=
ENST00000346085.9:c.4494T>C	ENSP00000344546.4:p.Asp1498=
ENST00000350026.9:c.4455T>C	ENSP00000055163.7:p.Asp1485=
ENST00000414678.6:c.3021T>C	ENSP00000412835.2:p.Asp1007=
NM_017519.2:c.4455T>C	NP_059989.2:p.Asp1485=
NM_020732.3:c.4494T>C	NP_065783.3:p.Asp1498=
XM_005267069.3:c.4614T>C	XP_005267126.2:p.Asp1538=
XM_011535984.1:c.3693T>C	XP_011534286.1:p.Asp1231=
XM_011535985.1:c.3513T>C	XP_011534287.1:p.Asp1171=
XM_011535986.1:c.3273T>C	XP_011534288.1:p.Asp1091=
XM_011535987.1:c.2892T>C	XP_011534289.1:p.Asp964=
XM_011535988.1:c.1755T>C	XP_011534290.1:p.Asp585=
NM_001346813.1:c.4614T>C	NP_001333742.1:p.Asp1538=
NM_001363725.1:c.2364T>C	NP_001350654.1:p.Asp788=
XM_011535984.2:c.4824T>C	XP_011534286.2:p.Asp1608=
XM_011535988.3:c.1755T>C	XP_011534290.1:p.Asp585=
XM_017011103.2:c.4725T>C	XP_016866592.1:p.Asp1575=
XM_017011104.1:c.4695T>C	XP_016866593.1:p.Asp1565=
XM_017011105.2:c.4665T>C	XP_016866594.1:p.Asp1555=
XM_017011106.2:c.4536T>C	XP_016866595.1:p.Asp1512=
XM_017011107.2:c.4515T>C	XP_016866596.1:p.Asp1505=
XR_002956289.1:n.4810T>C
NM_001363725.2:c.2364T>C	NP_001350654.1:p.Asp788=
NM_001371656.1:c.4743T>C	NP_001358585.1:p.Asp1581=
NM_001374820.1:c.4743T>C	NP_001361749.1:p.Asp1581=
NM_001374828.1:c.4863T>C MANE Select	NP_001361757.1:p.Asp1621=
NM_017519.3:c.4704T>C	NP_059989.3:p.Asp1568=