Canonical Allele Identifier: CA452781575

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510909T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189775T>C , CM000668.2:g.157189775T>C	GRCh38
NC_000006.11:g.157510909T>C , CM000668.1:g.157510909T>C	GRCh37
NC_000006.10:g.157552601T>C	NCBI36
NG_032093.1:g.416846T>C
NG_032093.2:g.416846T>C
NG_066624.1:g.418750T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3894T>C	ENSP00000055163.8:p.Gly1298=
ENST00000414678.8:c.3963T>C	ENSP00000412835.3:p.Gly1321=
ENST00000637015.2:c.4182T>C	ENSP00000489729.2:p.Gly1394=
ENST00000346085.10:c.3933T>C	ENSP00000344546.5:p.Gly1311=
ENST00000350026.10:c.3645T>C	ENSP00000055163.7:p.Gly1215=
ENST00000414678.7:c.2211T>C	ENSP00000412835.2:p.Gly737=
ENST00000635849.1:c.1374T>C	ENSP00000490948.1:p.Gly458=
ENST00000635957.1:c.1008T>C	ENSP00000490385.1:p.Gly336=
ENST00000636930.2:c.4053T>C MANE Select	ENSP00000490491.2:p.Gly1351=
ENST00000636940.1:n.2050T>C
ENST00000637015.1:c.1421T>C
ENST00000637568.1:c.1335T>C
ENST00000637741.1:n.719T>C
ENST00000637810.1:c.1395T>C	ENSP00000489636.1:p.Gly465=
ENST00000637904.1:c.1554T>C	ENSP00000490550.1:p.Gly518=
ENST00000647938.1:c.3684T>C	ENSP00000498155.1:p.Gly1228=
ENST00000346085.9:c.3684T>C	ENSP00000344546.4:p.Gly1228=
ENST00000350026.9:c.3645T>C	ENSP00000055163.7:p.Gly1215=
ENST00000414678.6:c.2211T>C	ENSP00000412835.2:p.Gly737=
NM_017519.2:c.3645T>C	NP_059989.2:p.Gly1215=
NM_020732.3:c.3684T>C	NP_065783.3:p.Gly1228=
XM_005267069.3:c.3804T>C	XP_005267126.2:p.Gly1268=
XM_011535984.1:c.2883T>C	XP_011534286.1:p.Gly961=
XM_011535985.1:c.2703T>C	XP_011534287.1:p.Gly901=
XM_011535986.1:c.2463T>C	XP_011534288.1:p.Gly821=
XM_011535987.1:c.2082T>C	XP_011534289.1:p.Gly694=
XM_011535988.1:c.945T>C	XP_011534290.1:p.Gly315=
NM_001346813.1:c.3804T>C	NP_001333742.1:p.Gly1268=
NM_001363725.1:c.1554T>C	NP_001350654.1:p.Gly518=
XM_011535984.2:c.4014T>C	XP_011534286.2:p.Gly1338=
XM_011535988.3:c.945T>C	XP_011534290.1:p.Gly315=
XM_017011103.2:c.3915T>C	XP_016866592.1:p.Gly1305=
XM_017011104.1:c.3885T>C	XP_016866593.1:p.Gly1295=
XM_017011105.2:c.3855T>C	XP_016866594.1:p.Gly1285=
XM_017011106.2:c.3726T>C	XP_016866595.1:p.Gly1242=
XM_017011107.2:c.3705T>C	XP_016866596.1:p.Gly1235=
XR_002956289.1:n.4097T>C
NM_001363725.2:c.1554T>C	NP_001350654.1:p.Gly518=
NM_001371656.1:c.3933T>C	NP_001358585.1:p.Gly1311=
NM_001374820.1:c.3933T>C	NP_001361749.1:p.Gly1311=
NM_001374828.1:c.4053T>C MANE Select	NP_001361757.1:p.Gly1351=
NM_017519.3:c.3894T>C	NP_059989.3:p.Gly1298=