Canonical Allele Identifier: CA366234393

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510907G>C (hg19) ; chr6:g.157189773G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189773G>C , CM000668.2:g.157189773G>C	GRCh38
NC_000006.11:g.157510907G>C , CM000668.1:g.157510907G>C	GRCh37
NC_000006.10:g.157552599G>C	NCBI36
NG_032093.1:g.416844G>C
NG_032093.2:g.416844G>C
NG_066624.1:g.418748G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3892G>C	ENSP00000055163.8:p.Gly1298Arg
ENST00000414678.8:c.3961G>C	ENSP00000412835.3:p.Gly1321Arg
ENST00000637015.2:c.4180G>C	ENSP00000489729.2:p.Gly1394Arg
ENST00000346085.10:c.3931G>C	ENSP00000344546.5:p.Gly1311Arg
ENST00000350026.10:c.3643G>C	ENSP00000055163.7:p.Gly1215Arg
ENST00000414678.7:c.2209G>C	ENSP00000412835.2:p.Gly737Arg
ENST00000635849.1:c.1372G>C	ENSP00000490948.1:p.Gly458Arg
ENST00000635957.1:c.1006G>C	ENSP00000490385.1:p.Gly336Arg
ENST00000636930.2:c.4051G>C MANE Select	ENSP00000490491.2:p.Gly1351Arg
ENST00000636940.1:n.2048G>C
ENST00000637015.1:c.1419G>C
ENST00000637568.1:c.1333G>C
ENST00000637741.1:n.717G>C
ENST00000637810.1:c.1393G>C	ENSP00000489636.1:p.Gly465Arg
ENST00000637904.1:c.1552G>C	ENSP00000490550.1:p.Gly518Arg
ENST00000647938.1:c.3682G>C	ENSP00000498155.1:p.Gly1228Arg
ENST00000346085.9:c.3682G>C	ENSP00000344546.4:p.Gly1228Arg
ENST00000350026.9:c.3643G>C	ENSP00000055163.7:p.Gly1215Arg
ENST00000414678.6:c.2209G>C	ENSP00000412835.2:p.Gly737Arg
NM_017519.2:c.3643G>C	NP_059989.2:p.Gly1215Arg
NM_020732.3:c.3682G>C	NP_065783.3:p.Gly1228Arg
XM_005267069.3:c.3802G>C	XP_005267126.2:p.Gly1268Arg
XM_011535984.1:c.2881G>C	XP_011534286.1:p.Gly961Arg
XM_011535985.1:c.2701G>C	XP_011534287.1:p.Gly901Arg
XM_011535986.1:c.2461G>C	XP_011534288.1:p.Gly821Arg
XM_011535987.1:c.2080G>C	XP_011534289.1:p.Gly694Arg
XM_011535988.1:c.943G>C	XP_011534290.1:p.Gly315Arg
NM_001346813.1:c.3802G>C	NP_001333742.1:p.Gly1268Arg
NM_001363725.1:c.1552G>C	NP_001350654.1:p.Gly518Arg
XM_011535984.2:c.4012G>C	XP_011534286.2:p.Gly1338Arg
XM_011535988.3:c.943G>C	XP_011534290.1:p.Gly315Arg
XM_017011103.2:c.3913G>C	XP_016866592.1:p.Gly1305Arg
XM_017011104.1:c.3883G>C	XP_016866593.1:p.Gly1295Arg
XM_017011105.2:c.3853G>C	XP_016866594.1:p.Gly1285Arg
XM_017011106.2:c.3724G>C	XP_016866595.1:p.Gly1242Arg
XM_017011107.2:c.3703G>C	XP_016866596.1:p.Gly1235Arg
XR_002956289.1:n.4095G>C
NM_001363725.2:c.1552G>C	NP_001350654.1:p.Gly518Arg
NM_001371656.1:c.3931G>C	NP_001358585.1:p.Gly1311Arg
NM_001374820.1:c.3931G>C	NP_001361749.1:p.Gly1311Arg
NM_001374828.1:c.4051G>C MANE Select	NP_001361757.1:p.Gly1351Arg
NM_017519.3:c.3892G>C	NP_059989.3:p.Gly1298Arg