Canonical Allele Identifier: CA366234351

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510903G>T (hg19) ; chr6:g.157189769G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189769G>T , CM000668.2:g.157189769G>T	GRCh38
NC_000006.11:g.157510903G>T , CM000668.1:g.157510903G>T	GRCh37
NC_000006.10:g.157552595G>T	NCBI36
NG_032093.1:g.416840G>T
NG_032093.2:g.416840G>T
NG_066624.1:g.418744G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3888G>T	ENSP00000055163.8:p.Met1296Ile
ENST00000414678.8:c.3957G>T	ENSP00000412835.3:p.Met1319Ile
ENST00000637015.2:c.4176G>T	ENSP00000489729.2:p.Met1392Ile
ENST00000346085.10:c.3927G>T	ENSP00000344546.5:p.Met1309Ile
ENST00000350026.10:c.3639G>T	ENSP00000055163.7:p.Met1213Ile
ENST00000414678.7:c.2205G>T	ENSP00000412835.2:p.Met735Ile
ENST00000635849.1:c.1368G>T	ENSP00000490948.1:p.Met456Ile
ENST00000635957.1:c.1002G>T	ENSP00000490385.1:p.Met334Ile
ENST00000636930.2:c.4047G>T MANE Select	ENSP00000490491.2:p.Met1349Ile
ENST00000636940.1:n.2044G>T
ENST00000637015.1:c.1415G>T
ENST00000637568.1:c.1329G>T
ENST00000637741.1:n.713G>T
ENST00000637810.1:c.1389G>T	ENSP00000489636.1:p.Met463Ile
ENST00000637904.1:c.1548G>T	ENSP00000490550.1:p.Met516Ile
ENST00000647938.1:c.3678G>T	ENSP00000498155.1:p.Met1226Ile
ENST00000346085.9:c.3678G>T	ENSP00000344546.4:p.Met1226Ile
ENST00000350026.9:c.3639G>T	ENSP00000055163.7:p.Met1213Ile
ENST00000414678.6:c.2205G>T	ENSP00000412835.2:p.Met735Ile
NM_017519.2:c.3639G>T	NP_059989.2:p.Met1213Ile
NM_020732.3:c.3678G>T	NP_065783.3:p.Met1226Ile
XM_005267069.3:c.3798G>T	XP_005267126.2:p.Met1266Ile
XM_011535984.1:c.2877G>T	XP_011534286.1:p.Met959Ile
XM_011535985.1:c.2697G>T	XP_011534287.1:p.Met899Ile
XM_011535986.1:c.2457G>T	XP_011534288.1:p.Met819Ile
XM_011535987.1:c.2076G>T	XP_011534289.1:p.Met692Ile
XM_011535988.1:c.939G>T	XP_011534290.1:p.Met313Ile
NM_001346813.1:c.3798G>T	NP_001333742.1:p.Met1266Ile
NM_001363725.1:c.1548G>T	NP_001350654.1:p.Met516Ile
XM_011535984.2:c.4008G>T	XP_011534286.2:p.Met1336Ile
XM_011535988.3:c.939G>T	XP_011534290.1:p.Met313Ile
XM_017011103.2:c.3909G>T	XP_016866592.1:p.Met1303Ile
XM_017011104.1:c.3879G>T	XP_016866593.1:p.Met1293Ile
XM_017011105.2:c.3849G>T	XP_016866594.1:p.Met1283Ile
XM_017011106.2:c.3720G>T	XP_016866595.1:p.Met1240Ile
XM_017011107.2:c.3699G>T	XP_016866596.1:p.Met1233Ile
XR_002956289.1:n.4091G>T
NM_001363725.2:c.1548G>T	NP_001350654.1:p.Met516Ile
NM_001371656.1:c.3927G>T	NP_001358585.1:p.Met1309Ile
NM_001374820.1:c.3927G>T	NP_001361749.1:p.Met1309Ile
NM_001374828.1:c.4047G>T MANE Select	NP_001361757.1:p.Met1349Ile
NM_017519.3:c.3888G>T	NP_059989.3:p.Met1296Ile