Canonical Allele Identifier: CA366242347

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522392G>C (hg19) ; chr6:g.157201258G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201258G>C , CM000668.2:g.157201258G>C	GRCh38
NC_000006.11:g.157522392G>C , CM000668.1:g.157522392G>C	GRCh37
NC_000006.10:g.157564084G>C	NCBI36
NG_032093.1:g.428329G>C
NG_032093.2:g.428329G>C
NG_066624.1:g.430233G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4874G>C	ENSP00000055163.8:p.Ser1625Thr
ENST00000414678.8:c.4943G>C	ENSP00000412835.3:p.Ser1648Thr
ENST00000637015.2:c.5162G>C	ENSP00000489729.2:p.Ser1721Thr
ENST00000346085.10:c.4913G>C	ENSP00000344546.5:p.Ser1638Thr
ENST00000350026.10:c.4625G>C	ENSP00000055163.7:p.Ser1542Thr
ENST00000414678.7:c.3191G>C	ENSP00000412835.2:p.Ser1064Thr
ENST00000635849.1:c.2354G>C	ENSP00000490948.1:p.Ser785Thr
ENST00000635957.1:c.1985G>C	ENSP00000490385.1:p.Ser662Thr
ENST00000636227.1:n.3496G>C
ENST00000636254.1:n.953G>C
ENST00000636930.2:c.5033G>C MANE Select	ENSP00000490491.2:p.Ser1678Thr
ENST00000636940.1:n.3030G>C
ENST00000637015.1:c.2401G>C
ENST00000637568.1:c.2315G>C
ENST00000637741.1:n.1699G>C
ENST00000637810.1:c.2375G>C	ENSP00000489636.1:p.Ser792Thr
ENST00000637904.1:c.2534G>C	ENSP00000490550.1:p.Ser845Thr
ENST00000647938.1:c.4664G>C	ENSP00000498155.1:p.Ser1555Thr
ENST00000346085.9:c.4664G>C	ENSP00000344546.4:p.Ser1555Thr
ENST00000350026.9:c.4625G>C	ENSP00000055163.7:p.Ser1542Thr
ENST00000414678.6:c.3191G>C	ENSP00000412835.2:p.Ser1064Thr
NM_017519.2:c.4625G>C	NP_059989.2:p.Ser1542Thr
NM_020732.3:c.4664G>C	NP_065783.3:p.Ser1555Thr
XM_005267069.3:c.4784G>C	XP_005267126.2:p.Ser1595Thr
XM_011535984.1:c.3863G>C	XP_011534286.1:p.Ser1288Thr
XM_011535985.1:c.3683G>C	XP_011534287.1:p.Ser1228Thr
XM_011535986.1:c.3443G>C	XP_011534288.1:p.Ser1148Thr
XM_011535987.1:c.3062G>C	XP_011534289.1:p.Ser1021Thr
XM_011535988.1:c.1925G>C	XP_011534290.1:p.Ser642Thr
NM_001346813.1:c.4784G>C	NP_001333742.1:p.Ser1595Thr
NM_001363725.1:c.2534G>C	NP_001350654.1:p.Ser845Thr
XM_011535984.2:c.4994G>C	XP_011534286.2:p.Ser1665Thr
XM_011535988.3:c.1925G>C	XP_011534290.1:p.Ser642Thr
XM_017011103.2:c.4895G>C	XP_016866592.1:p.Ser1632Thr
XM_017011104.1:c.4865G>C	XP_016866593.1:p.Ser1622Thr
XM_017011105.2:c.4835G>C	XP_016866594.1:p.Ser1612Thr
XM_017011106.2:c.4706G>C	XP_016866595.1:p.Ser1569Thr
XM_017011107.2:c.4685G>C	XP_016866596.1:p.Ser1562Thr
XR_002956289.1:n.4980G>C
NM_001363725.2:c.2534G>C	NP_001350654.1:p.Ser845Thr
NM_001371656.1:c.4913G>C	NP_001358585.1:p.Ser1638Thr
NM_001374820.1:c.4913G>C	NP_001361749.1:p.Ser1638Thr
NM_001374828.1:c.5033G>C MANE Select	NP_001361757.1:p.Ser1678Thr
NM_017519.3:c.4874G>C	NP_059989.3:p.Ser1625Thr