Canonical Allele Identifier: CA366242145

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522296T>C (hg19) ; chr6:g.157201162T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201162T>C , CM000668.2:g.157201162T>C	GRCh38
NC_000006.11:g.157522296T>C , CM000668.1:g.157522296T>C	GRCh37
NC_000006.10:g.157563988T>C	NCBI36
NG_032093.1:g.428233T>C
NG_032093.2:g.428233T>C
NG_066624.1:g.430137T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4778T>C	ENSP00000055163.8:p.Met1593Thr
ENST00000414678.8:c.4847T>C	ENSP00000412835.3:p.Met1616Thr
ENST00000637015.2:c.5066T>C	ENSP00000489729.2:p.Met1689Thr
ENST00000346085.10:c.4817T>C	ENSP00000344546.5:p.Met1606Thr
ENST00000350026.10:c.4529T>C	ENSP00000055163.7:p.Met1510Thr
ENST00000414678.7:c.3095T>C	ENSP00000412835.2:p.Met1032Thr
ENST00000635849.1:c.2258T>C	ENSP00000490948.1:p.Met753Thr
ENST00000635957.1:c.1889T>C	ENSP00000490385.1:p.Met630Thr
ENST00000636227.1:n.3400T>C
ENST00000636254.1:n.857T>C
ENST00000636930.2:c.4937T>C MANE Select	ENSP00000490491.2:p.Met1646Thr
ENST00000636940.1:n.2934T>C
ENST00000637015.1:c.2305T>C
ENST00000637568.1:c.2219T>C
ENST00000637741.1:n.1603T>C
ENST00000637810.1:c.2279T>C	ENSP00000489636.1:p.Met760Thr
ENST00000637904.1:c.2438T>C	ENSP00000490550.1:p.Met813Thr
ENST00000647938.1:c.4568T>C	ENSP00000498155.1:p.Met1523Thr
ENST00000346085.9:c.4568T>C	ENSP00000344546.4:p.Met1523Thr
ENST00000350026.9:c.4529T>C	ENSP00000055163.7:p.Met1510Thr
ENST00000414678.6:c.3095T>C	ENSP00000412835.2:p.Met1032Thr
NM_017519.2:c.4529T>C	NP_059989.2:p.Met1510Thr
NM_020732.3:c.4568T>C	NP_065783.3:p.Met1523Thr
XM_005267069.3:c.4688T>C	XP_005267126.2:p.Met1563Thr
XM_011535984.1:c.3767T>C	XP_011534286.1:p.Met1256Thr
XM_011535985.1:c.3587T>C	XP_011534287.1:p.Met1196Thr
XM_011535986.1:c.3347T>C	XP_011534288.1:p.Met1116Thr
XM_011535987.1:c.2966T>C	XP_011534289.1:p.Met989Thr
XM_011535988.1:c.1829T>C	XP_011534290.1:p.Met610Thr
NM_001346813.1:c.4688T>C	NP_001333742.1:p.Met1563Thr
NM_001363725.1:c.2438T>C	NP_001350654.1:p.Met813Thr
XM_011535984.2:c.4898T>C	XP_011534286.2:p.Met1633Thr
XM_011535988.3:c.1829T>C	XP_011534290.1:p.Met610Thr
XM_017011103.2:c.4799T>C	XP_016866592.1:p.Met1600Thr
XM_017011104.1:c.4769T>C	XP_016866593.1:p.Met1590Thr
XM_017011105.2:c.4739T>C	XP_016866594.1:p.Met1580Thr
XM_017011106.2:c.4610T>C	XP_016866595.1:p.Met1537Thr
XM_017011107.2:c.4589T>C	XP_016866596.1:p.Met1530Thr
XR_002956289.1:n.4884T>C
NM_001363725.2:c.2438T>C	NP_001350654.1:p.Met813Thr
NM_001371656.1:c.4817T>C	NP_001358585.1:p.Met1606Thr
NM_001374820.1:c.4817T>C	NP_001361749.1:p.Met1606Thr
NM_001374828.1:c.4937T>C MANE Select	NP_001361757.1:p.Met1646Thr
NM_017519.3:c.4778T>C	NP_059989.3:p.Met1593Thr