Canonical Allele Identifier: CA366234725

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511186G>C (hg19) ; chr6:g.157190052G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190052G>C , CM000668.2:g.157190052G>C	GRCh38
NC_000006.11:g.157511186G>C , CM000668.1:g.157511186G>C	GRCh37
NC_000006.10:g.157552878G>C	NCBI36
NG_032093.1:g.417123G>C
NG_032093.2:g.417123G>C
NG_066624.1:g.419027G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3914G>C	ENSP00000055163.8:p.Ser1305Thr
ENST00000414678.8:c.3983G>C	ENSP00000412835.3:p.Ser1328Thr
ENST00000637015.2:c.4202G>C	ENSP00000489729.2:p.Ser1401Thr
ENST00000346085.10:c.3953G>C	ENSP00000344546.5:p.Ser1318Thr
ENST00000350026.10:c.3665G>C	ENSP00000055163.7:p.Ser1222Thr
ENST00000414678.7:c.2231G>C	ENSP00000412835.2:p.Ser744Thr
ENST00000635849.1:c.1394G>C	ENSP00000490948.1:p.Ser465Thr
ENST00000635957.1:c.1025G>C	ENSP00000490385.1:p.Ser342Thr
ENST00000636930.2:c.4073G>C MANE Select	ENSP00000490491.2:p.Ser1358Thr
ENST00000636940.1:n.2070G>C
ENST00000637015.1:c.1441G>C
ENST00000637568.1:c.1355G>C
ENST00000637741.1:n.739G>C
ENST00000637810.1:c.1415G>C	ENSP00000489636.1:p.Ser472Thr
ENST00000637904.1:c.1574G>C	ENSP00000490550.1:p.Ser525Thr
ENST00000647938.1:c.3704G>C	ENSP00000498155.1:p.Ser1235Thr
ENST00000346085.9:c.3704G>C	ENSP00000344546.4:p.Ser1235Thr
ENST00000350026.9:c.3665G>C	ENSP00000055163.7:p.Ser1222Thr
ENST00000414678.6:c.2231G>C	ENSP00000412835.2:p.Ser744Thr
NM_017519.2:c.3665G>C	NP_059989.2:p.Ser1222Thr
NM_020732.3:c.3704G>C	NP_065783.3:p.Ser1235Thr
XM_005267069.3:c.3824G>C	XP_005267126.2:p.Ser1275Thr
XM_011535984.1:c.2903G>C	XP_011534286.1:p.Ser968Thr
XM_011535985.1:c.2723G>C	XP_011534287.1:p.Ser908Thr
XM_011535986.1:c.2483G>C	XP_011534288.1:p.Ser828Thr
XM_011535987.1:c.2102G>C	XP_011534289.1:p.Ser701Thr
XM_011535988.1:c.965G>C	XP_011534290.1:p.Ser322Thr
NM_001346813.1:c.3824G>C	NP_001333742.1:p.Ser1275Thr
NM_001363725.1:c.1574G>C	NP_001350654.1:p.Ser525Thr
XM_011535984.2:c.4034G>C	XP_011534286.2:p.Ser1345Thr
XM_011535988.3:c.965G>C	XP_011534290.1:p.Ser322Thr
XM_017011103.2:c.3935G>C	XP_016866592.1:p.Ser1312Thr
XM_017011104.1:c.3905G>C	XP_016866593.1:p.Ser1302Thr
XM_017011105.2:c.3875G>C	XP_016866594.1:p.Ser1292Thr
XM_017011106.2:c.3746G>C	XP_016866595.1:p.Ser1249Thr
XM_017011107.2:c.3725G>C	XP_016866596.1:p.Ser1242Thr
XR_002956289.1:n.4117G>C
NM_001363725.2:c.1574G>C	NP_001350654.1:p.Ser525Thr
NM_001371656.1:c.3953G>C	NP_001358585.1:p.Ser1318Thr
NM_001374820.1:c.3953G>C	NP_001361749.1:p.Ser1318Thr
NM_001374828.1:c.4073G>C MANE Select	NP_001361757.1:p.Ser1358Thr
NM_017519.3:c.3914G>C	NP_059989.3:p.Ser1305Thr