Canonical Allele Identifier: CA366234328

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510901A>C (hg19) ; chr6:g.157189767A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189767A>C , CM000668.2:g.157189767A>C	GRCh38
NC_000006.11:g.157510901A>C , CM000668.1:g.157510901A>C	GRCh37
NC_000006.10:g.157552593A>C	NCBI36
NG_032093.1:g.416838A>C
NG_032093.2:g.416838A>C
NG_066624.1:g.418742A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3886A>C	ENSP00000055163.8:p.Met1296Leu
ENST00000414678.8:c.3955A>C	ENSP00000412835.3:p.Met1319Leu
ENST00000637015.2:c.4174A>C	ENSP00000489729.2:p.Met1392Leu
ENST00000346085.10:c.3925A>C	ENSP00000344546.5:p.Met1309Leu
ENST00000350026.10:c.3637A>C	ENSP00000055163.7:p.Met1213Leu
ENST00000414678.7:c.2203A>C	ENSP00000412835.2:p.Met735Leu
ENST00000635849.1:c.1366A>C	ENSP00000490948.1:p.Met456Leu
ENST00000635957.1:c.1000A>C	ENSP00000490385.1:p.Met334Leu
ENST00000636930.2:c.4045A>C MANE Select	ENSP00000490491.2:p.Met1349Leu
ENST00000636940.1:n.2042A>C
ENST00000637015.1:c.1413A>C
ENST00000637568.1:c.1327A>C
ENST00000637741.1:n.711A>C
ENST00000637810.1:c.1387A>C	ENSP00000489636.1:p.Met463Leu
ENST00000637904.1:c.1546A>C	ENSP00000490550.1:p.Met516Leu
ENST00000647938.1:c.3676A>C	ENSP00000498155.1:p.Met1226Leu
ENST00000346085.9:c.3676A>C	ENSP00000344546.4:p.Met1226Leu
ENST00000350026.9:c.3637A>C	ENSP00000055163.7:p.Met1213Leu
ENST00000414678.6:c.2203A>C	ENSP00000412835.2:p.Met735Leu
NM_017519.2:c.3637A>C	NP_059989.2:p.Met1213Leu
NM_020732.3:c.3676A>C	NP_065783.3:p.Met1226Leu
XM_005267069.3:c.3796A>C	XP_005267126.2:p.Met1266Leu
XM_011535984.1:c.2875A>C	XP_011534286.1:p.Met959Leu
XM_011535985.1:c.2695A>C	XP_011534287.1:p.Met899Leu
XM_011535986.1:c.2455A>C	XP_011534288.1:p.Met819Leu
XM_011535987.1:c.2074A>C	XP_011534289.1:p.Met692Leu
XM_011535988.1:c.937A>C	XP_011534290.1:p.Met313Leu
NM_001346813.1:c.3796A>C	NP_001333742.1:p.Met1266Leu
NM_001363725.1:c.1546A>C	NP_001350654.1:p.Met516Leu
XM_011535984.2:c.4006A>C	XP_011534286.2:p.Met1336Leu
XM_011535988.3:c.937A>C	XP_011534290.1:p.Met313Leu
XM_017011103.2:c.3907A>C	XP_016866592.1:p.Met1303Leu
XM_017011104.1:c.3877A>C	XP_016866593.1:p.Met1293Leu
XM_017011105.2:c.3847A>C	XP_016866594.1:p.Met1283Leu
XM_017011106.2:c.3718A>C	XP_016866595.1:p.Met1240Leu
XM_017011107.2:c.3697A>C	XP_016866596.1:p.Met1233Leu
XR_002956289.1:n.4089A>C
NM_001363725.2:c.1546A>C	NP_001350654.1:p.Met516Leu
NM_001371656.1:c.3925A>C	NP_001358585.1:p.Met1309Leu
NM_001374820.1:c.3925A>C	NP_001361749.1:p.Met1309Leu
NM_001374828.1:c.4045A>C MANE Select	NP_001361757.1:p.Met1349Leu
NM_017519.3:c.3886A>C	NP_059989.3:p.Met1296Leu