Canonical Allele Identifier: CA366242922

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522532A>T (hg19) ; chr6:g.157201398A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201398A>T , CM000668.2:g.157201398A>T	GRCh38
NC_000006.11:g.157522532A>T , CM000668.1:g.157522532A>T	GRCh37
NC_000006.10:g.157564224A>T	NCBI36
NG_032093.1:g.428469A>T
NG_032093.2:g.428469A>T
NG_066624.1:g.430373A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5014A>T	ENSP00000055163.8:p.Ile1672Phe
ENST00000414678.8:c.5083A>T	ENSP00000412835.3:p.Ile1695Phe
ENST00000637015.2:c.5302A>T	ENSP00000489729.2:p.Ile1768Phe
ENST00000346085.10:c.5053A>T	ENSP00000344546.5:p.Ile1685Phe
ENST00000350026.10:c.4765A>T	ENSP00000055163.7:p.Ile1589Phe
ENST00000414678.7:c.3331A>T	ENSP00000412835.2:p.Ile1111Phe
ENST00000635849.1:c.2494A>T	ENSP00000490948.1:p.Ile832Phe
ENST00000635957.1:c.2125A>T	ENSP00000490385.1:p.Ile709Phe
ENST00000636227.1:n.3636A>T
ENST00000636254.1:n.1093A>T
ENST00000636930.2:c.5173A>T MANE Select	ENSP00000490491.2:p.Ile1725Phe
ENST00000636940.1:n.3170A>T
ENST00000637015.1:c.2541A>T
ENST00000637568.1:c.2455A>T
ENST00000637741.1:n.1839A>T
ENST00000637810.1:c.2515A>T	ENSP00000489636.1:p.Ile839Phe
ENST00000637904.1:c.2674A>T	ENSP00000490550.1:p.Ile892Phe
ENST00000647938.1:c.4804A>T	ENSP00000498155.1:p.Ile1602Phe
ENST00000346085.9:c.4804A>T	ENSP00000344546.4:p.Ile1602Phe
ENST00000350026.9:c.4765A>T	ENSP00000055163.7:p.Ile1589Phe
ENST00000414678.6:c.3331A>T	ENSP00000412835.2:p.Ile1111Phe
NM_017519.2:c.4765A>T	NP_059989.2:p.Ile1589Phe
NM_020732.3:c.4804A>T	NP_065783.3:p.Ile1602Phe
XM_005267069.3:c.4924A>T	XP_005267126.2:p.Ile1642Phe
XM_011535984.1:c.4003A>T	XP_011534286.1:p.Ile1335Phe
XM_011535985.1:c.3823A>T	XP_011534287.1:p.Ile1275Phe
XM_011535986.1:c.3583A>T	XP_011534288.1:p.Ile1195Phe
XM_011535987.1:c.3202A>T	XP_011534289.1:p.Ile1068Phe
XM_011535988.1:c.2065A>T	XP_011534290.1:p.Ile689Phe
NM_001346813.1:c.4924A>T	NP_001333742.1:p.Ile1642Phe
NM_001363725.1:c.2674A>T	NP_001350654.1:p.Ile892Phe
XM_011535984.2:c.5134A>T	XP_011534286.2:p.Ile1712Phe
XM_011535988.3:c.2065A>T	XP_011534290.1:p.Ile689Phe
XM_017011103.2:c.5035A>T	XP_016866592.1:p.Ile1679Phe
XM_017011104.1:c.5005A>T	XP_016866593.1:p.Ile1669Phe
XM_017011105.2:c.4975A>T	XP_016866594.1:p.Ile1659Phe
XM_017011106.2:c.4846A>T	XP_016866595.1:p.Ile1616Phe
XM_017011107.2:c.4825A>T	XP_016866596.1:p.Ile1609Phe
XR_002956289.1:n.5120A>T
NM_001363725.2:c.2674A>T	NP_001350654.1:p.Ile892Phe
NM_001371656.1:c.5053A>T	NP_001358585.1:p.Ile1685Phe
NM_001374820.1:c.5053A>T	NP_001361749.1:p.Ile1685Phe
NM_001374828.1:c.5173A>T MANE Select	NP_001361757.1:p.Ile1725Phe
NM_017519.3:c.5014A>T	NP_059989.3:p.Ile1672Phe