Canonical Allele Identifier: CA366242547

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522461T>C (hg19) ; chr6:g.157201327T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201327T>C , CM000668.2:g.157201327T>C	GRCh38
NC_000006.11:g.157522461T>C , CM000668.1:g.157522461T>C	GRCh37
NC_000006.10:g.157564153T>C	NCBI36
NG_032093.1:g.428398T>C
NG_032093.2:g.428398T>C
NG_066624.1:g.430302T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4943T>C	ENSP00000055163.8:p.Met1648Thr
ENST00000414678.8:c.5012T>C	ENSP00000412835.3:p.Met1671Thr
ENST00000637015.2:c.5231T>C	ENSP00000489729.2:p.Met1744Thr
ENST00000346085.10:c.4982T>C	ENSP00000344546.5:p.Met1661Thr
ENST00000350026.10:c.4694T>C	ENSP00000055163.7:p.Met1565Thr
ENST00000414678.7:c.3260T>C	ENSP00000412835.2:p.Met1087Thr
ENST00000635849.1:c.2423T>C	ENSP00000490948.1:p.Met808Thr
ENST00000635957.1:c.2054T>C	ENSP00000490385.1:p.Met685Thr
ENST00000636227.1:n.3565T>C
ENST00000636254.1:n.1022T>C
ENST00000636930.2:c.5102T>C MANE Select	ENSP00000490491.2:p.Met1701Thr
ENST00000636940.1:n.3099T>C
ENST00000637015.1:c.2470T>C
ENST00000637568.1:c.2384T>C
ENST00000637741.1:n.1768T>C
ENST00000637810.1:c.2444T>C	ENSP00000489636.1:p.Met815Thr
ENST00000637904.1:c.2603T>C	ENSP00000490550.1:p.Met868Thr
ENST00000647938.1:c.4733T>C	ENSP00000498155.1:p.Met1578Thr
ENST00000346085.9:c.4733T>C	ENSP00000344546.4:p.Met1578Thr
ENST00000350026.9:c.4694T>C	ENSP00000055163.7:p.Met1565Thr
ENST00000414678.6:c.3260T>C	ENSP00000412835.2:p.Met1087Thr
NM_017519.2:c.4694T>C	NP_059989.2:p.Met1565Thr
NM_020732.3:c.4733T>C	NP_065783.3:p.Met1578Thr
XM_005267069.3:c.4853T>C	XP_005267126.2:p.Met1618Thr
XM_011535984.1:c.3932T>C	XP_011534286.1:p.Met1311Thr
XM_011535985.1:c.3752T>C	XP_011534287.1:p.Met1251Thr
XM_011535986.1:c.3512T>C	XP_011534288.1:p.Met1171Thr
XM_011535987.1:c.3131T>C	XP_011534289.1:p.Met1044Thr
XM_011535988.1:c.1994T>C	XP_011534290.1:p.Met665Thr
NM_001346813.1:c.4853T>C	NP_001333742.1:p.Met1618Thr
NM_001363725.1:c.2603T>C	NP_001350654.1:p.Met868Thr
XM_011535984.2:c.5063T>C	XP_011534286.2:p.Met1688Thr
XM_011535988.3:c.1994T>C	XP_011534290.1:p.Met665Thr
XM_017011103.2:c.4964T>C	XP_016866592.1:p.Met1655Thr
XM_017011104.1:c.4934T>C	XP_016866593.1:p.Met1645Thr
XM_017011105.2:c.4904T>C	XP_016866594.1:p.Met1635Thr
XM_017011106.2:c.4775T>C	XP_016866595.1:p.Met1592Thr
XM_017011107.2:c.4754T>C	XP_016866596.1:p.Met1585Thr
XR_002956289.1:n.5049T>C
NM_001363725.2:c.2603T>C	NP_001350654.1:p.Met868Thr
NM_001371656.1:c.4982T>C	NP_001358585.1:p.Met1661Thr
NM_001374820.1:c.4982T>C	NP_001361749.1:p.Met1661Thr
NM_001374828.1:c.5102T>C MANE Select	NP_001361757.1:p.Met1701Thr
NM_017519.3:c.4943T>C	NP_059989.3:p.Met1648Thr