Canonical Allele Identifier: CA366234058

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510806C>G (hg19) ; chr6:g.157189672C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189672C>G , CM000668.2:g.157189672C>G	GRCh38
NC_000006.11:g.157510806C>G , CM000668.1:g.157510806C>G	GRCh37
NC_000006.10:g.157552498C>G	NCBI36
NG_032093.1:g.416743C>G
NG_032093.2:g.416743C>G
NG_066624.1:g.418647C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3791C>G	ENSP00000055163.8:p.Thr1264Ser
ENST00000414678.8:c.3860C>G	ENSP00000412835.3:p.Thr1287Ser
ENST00000637015.2:c.4079C>G	ENSP00000489729.2:p.Thr1360Ser
ENST00000346085.10:c.3830C>G	ENSP00000344546.5:p.Thr1277Ser
ENST00000350026.10:c.3542C>G	ENSP00000055163.7:p.Thr1181Ser
ENST00000414678.7:c.2108C>G	ENSP00000412835.2:p.Thr703Ser
ENST00000635849.1:c.1271C>G	ENSP00000490948.1:p.Thr424Ser
ENST00000635957.1:c.905C>G	ENSP00000490385.1:p.Thr302Ser
ENST00000636930.2:c.3950C>G MANE Select	ENSP00000490491.2:p.Thr1317Ser
ENST00000636940.1:n.1947C>G
ENST00000637015.1:c.1318C>G
ENST00000637568.1:c.1232C>G
ENST00000637741.1:n.616C>G
ENST00000637810.1:c.1292C>G	ENSP00000489636.1:p.Thr431Ser
ENST00000637904.1:c.1451C>G	ENSP00000490550.1:p.Thr484Ser
ENST00000647938.1:c.3581C>G	ENSP00000498155.1:p.Thr1194Ser
ENST00000346085.9:c.3581C>G	ENSP00000344546.4:p.Thr1194Ser
ENST00000350026.9:c.3542C>G	ENSP00000055163.7:p.Thr1181Ser
ENST00000414678.6:c.2108C>G	ENSP00000412835.2:p.Thr703Ser
NM_017519.2:c.3542C>G	NP_059989.2:p.Thr1181Ser
NM_020732.3:c.3581C>G	NP_065783.3:p.Thr1194Ser
XM_005267069.3:c.3701C>G	XP_005267126.2:p.Thr1234Ser
XM_011535984.1:c.2780C>G	XP_011534286.1:p.Thr927Ser
XM_011535985.1:c.2600C>G	XP_011534287.1:p.Thr867Ser
XM_011535986.1:c.2360C>G	XP_011534288.1:p.Thr787Ser
XM_011535987.1:c.1979C>G	XP_011534289.1:p.Thr660Ser
XM_011535988.1:c.842C>G	XP_011534290.1:p.Thr281Ser
NM_001346813.1:c.3701C>G	NP_001333742.1:p.Thr1234Ser
NM_001363725.1:c.1451C>G	NP_001350654.1:p.Thr484Ser
XM_011535984.2:c.3911C>G	XP_011534286.2:p.Thr1304Ser
XM_011535988.3:c.842C>G	XP_011534290.1:p.Thr281Ser
XM_017011103.2:c.3812C>G	XP_016866592.1:p.Thr1271Ser
XM_017011104.1:c.3782C>G	XP_016866593.1:p.Thr1261Ser
XM_017011105.2:c.3752C>G	XP_016866594.1:p.Thr1251Ser
XM_017011106.2:c.3623C>G	XP_016866595.1:p.Thr1208Ser
XM_017011107.2:c.3602C>G	XP_016866596.1:p.Thr1201Ser
XR_002956289.1:n.3994C>G
NM_001363725.2:c.1451C>G	NP_001350654.1:p.Thr484Ser
NM_001371656.1:c.3830C>G	NP_001358585.1:p.Thr1277Ser
NM_001374820.1:c.3830C>G	NP_001361749.1:p.Thr1277Ser
NM_001374828.1:c.3950C>G MANE Select	NP_001361757.1:p.Thr1317Ser
NM_017519.3:c.3791C>G	NP_059989.3:p.Thr1264Ser