Canonical Allele Identifier: CA366241872

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522214A>C (hg19) ; chr6:g.157201080A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201080A>C , CM000668.2:g.157201080A>C	GRCh38
NC_000006.11:g.157522214A>C , CM000668.1:g.157522214A>C	GRCh37
NC_000006.10:g.157563906A>C	NCBI36
NG_032093.1:g.428151A>C
NG_032093.2:g.428151A>C
NG_066624.1:g.430055A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4696A>C	ENSP00000055163.8:p.Thr1566Pro
ENST00000414678.8:c.4765A>C	ENSP00000412835.3:p.Thr1589Pro
ENST00000637015.2:c.4984A>C	ENSP00000489729.2:p.Thr1662Pro
ENST00000346085.10:c.4735A>C	ENSP00000344546.5:p.Thr1579Pro
ENST00000350026.10:c.4447A>C	ENSP00000055163.7:p.Thr1483Pro
ENST00000414678.7:c.3013A>C	ENSP00000412835.2:p.Thr1005Pro
ENST00000635849.1:c.2176A>C	ENSP00000490948.1:p.Thr726Pro
ENST00000635957.1:c.1807A>C	ENSP00000490385.1:p.Thr603Pro
ENST00000636227.1:n.3318A>C
ENST00000636254.1:n.775A>C
ENST00000636930.2:c.4855A>C MANE Select	ENSP00000490491.2:p.Thr1619Pro
ENST00000636940.1:n.2852A>C
ENST00000637015.1:c.2223A>C
ENST00000637568.1:c.2137A>C
ENST00000637741.1:n.1521A>C
ENST00000637810.1:c.2197A>C	ENSP00000489636.1:p.Thr733Pro
ENST00000637904.1:c.2356A>C	ENSP00000490550.1:p.Thr786Pro
ENST00000647938.1:c.4486A>C	ENSP00000498155.1:p.Thr1496Pro
ENST00000346085.9:c.4486A>C	ENSP00000344546.4:p.Thr1496Pro
ENST00000350026.9:c.4447A>C	ENSP00000055163.7:p.Thr1483Pro
ENST00000414678.6:c.3013A>C	ENSP00000412835.2:p.Thr1005Pro
NM_017519.2:c.4447A>C	NP_059989.2:p.Thr1483Pro
NM_020732.3:c.4486A>C	NP_065783.3:p.Thr1496Pro
XM_005267069.3:c.4606A>C	XP_005267126.2:p.Thr1536Pro
XM_011535984.1:c.3685A>C	XP_011534286.1:p.Thr1229Pro
XM_011535985.1:c.3505A>C	XP_011534287.1:p.Thr1169Pro
XM_011535986.1:c.3265A>C	XP_011534288.1:p.Thr1089Pro
XM_011535987.1:c.2884A>C	XP_011534289.1:p.Thr962Pro
XM_011535988.1:c.1747A>C	XP_011534290.1:p.Thr583Pro
NM_001346813.1:c.4606A>C	NP_001333742.1:p.Thr1536Pro
NM_001363725.1:c.2356A>C	NP_001350654.1:p.Thr786Pro
XM_011535984.2:c.4816A>C	XP_011534286.2:p.Thr1606Pro
XM_011535988.3:c.1747A>C	XP_011534290.1:p.Thr583Pro
XM_017011103.2:c.4717A>C	XP_016866592.1:p.Thr1573Pro
XM_017011104.1:c.4687A>C	XP_016866593.1:p.Thr1563Pro
XM_017011105.2:c.4657A>C	XP_016866594.1:p.Thr1553Pro
XM_017011106.2:c.4528A>C	XP_016866595.1:p.Thr1510Pro
XM_017011107.2:c.4507A>C	XP_016866596.1:p.Thr1503Pro
XR_002956289.1:n.4802A>C
NM_001363725.2:c.2356A>C	NP_001350654.1:p.Thr786Pro
NM_001371656.1:c.4735A>C	NP_001358585.1:p.Thr1579Pro
NM_001374820.1:c.4735A>C	NP_001361749.1:p.Thr1579Pro
NM_001374828.1:c.4855A>C MANE Select	NP_001361757.1:p.Thr1619Pro
NM_017519.3:c.4696A>C	NP_059989.3:p.Thr1566Pro