Canonical Allele Identifier: CA366241153

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522020G>C (hg19) ; chr6:g.157200886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200886G>C , CM000668.2:g.157200886G>C	GRCh38
NC_000006.11:g.157522020G>C , CM000668.1:g.157522020G>C	GRCh37
NC_000006.10:g.157563712G>C	NCBI36
NG_032093.1:g.427957G>C
NG_032093.2:g.427957G>C
NG_066624.1:g.429861G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4502G>C	ENSP00000055163.8:p.Arg1501Thr
ENST00000414678.8:c.4571G>C	ENSP00000412835.3:p.Arg1524Thr
ENST00000637015.2:c.4790G>C	ENSP00000489729.2:p.Arg1597Thr
ENST00000346085.10:c.4541G>C	ENSP00000344546.5:p.Arg1514Thr
ENST00000350026.10:c.4253G>C	ENSP00000055163.7:p.Arg1418Thr
ENST00000414678.7:c.2819G>C	ENSP00000412835.2:p.Arg940Thr
ENST00000635849.1:c.1982G>C	ENSP00000490948.1:p.Arg661Thr
ENST00000635957.1:c.1613G>C	ENSP00000490385.1:p.Arg538Thr
ENST00000636227.1:n.3124G>C
ENST00000636254.1:n.581G>C
ENST00000636930.2:c.4661G>C MANE Select	ENSP00000490491.2:p.Arg1554Thr
ENST00000636940.1:n.2658G>C
ENST00000637015.1:c.2029G>C
ENST00000637568.1:c.1943G>C
ENST00000637741.1:n.1327G>C
ENST00000637810.1:c.2003G>C	ENSP00000489636.1:p.Arg668Thr
ENST00000637904.1:c.2162G>C	ENSP00000490550.1:p.Arg721Thr
ENST00000647938.1:c.4292G>C	ENSP00000498155.1:p.Arg1431Thr
ENST00000346085.9:c.4292G>C	ENSP00000344546.4:p.Arg1431Thr
ENST00000350026.9:c.4253G>C	ENSP00000055163.7:p.Arg1418Thr
ENST00000414678.6:c.2819G>C	ENSP00000412835.2:p.Arg940Thr
NM_017519.2:c.4253G>C	NP_059989.2:p.Arg1418Thr
NM_020732.3:c.4292G>C	NP_065783.3:p.Arg1431Thr
XM_005267069.3:c.4412G>C	XP_005267126.2:p.Arg1471Thr
XM_011535984.1:c.3491G>C	XP_011534286.1:p.Arg1164Thr
XM_011535985.1:c.3311G>C	XP_011534287.1:p.Arg1104Thr
XM_011535986.1:c.3071G>C	XP_011534288.1:p.Arg1024Thr
XM_011535987.1:c.2690G>C	XP_011534289.1:p.Arg897Thr
XM_011535988.1:c.1553G>C	XP_011534290.1:p.Arg518Thr
NM_001346813.1:c.4412G>C	NP_001333742.1:p.Arg1471Thr
NM_001363725.1:c.2162G>C	NP_001350654.1:p.Arg721Thr
XM_011535984.2:c.4622G>C	XP_011534286.2:p.Arg1541Thr
XM_011535988.3:c.1553G>C	XP_011534290.1:p.Arg518Thr
XM_017011103.2:c.4523G>C	XP_016866592.1:p.Arg1508Thr
XM_017011104.1:c.4493G>C	XP_016866593.1:p.Arg1498Thr
XM_017011105.2:c.4463G>C	XP_016866594.1:p.Arg1488Thr
XM_017011106.2:c.4334G>C	XP_016866595.1:p.Arg1445Thr
XM_017011107.2:c.4313G>C	XP_016866596.1:p.Arg1438Thr
XR_002956289.1:n.4608G>C
NM_001363725.2:c.2162G>C	NP_001350654.1:p.Arg721Thr
NM_001371656.1:c.4541G>C	NP_001358585.1:p.Arg1514Thr
NM_001374820.1:c.4541G>C	NP_001361749.1:p.Arg1514Thr
NM_001374828.1:c.4661G>C MANE Select	NP_001361757.1:p.Arg1554Thr
NM_017519.3:c.4502G>C	NP_059989.3:p.Arg1501Thr