Canonical Allele Identifier: CA366234030

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510794A>C (hg19) ; chr6:g.157189660A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189660A>C , CM000668.2:g.157189660A>C	GRCh38
NC_000006.11:g.157510794A>C , CM000668.1:g.157510794A>C	GRCh37
NC_000006.10:g.157552486A>C	NCBI36
NG_032093.1:g.416731A>C
NG_032093.2:g.416731A>C
NG_066624.1:g.418635A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3779A>C	ENSP00000055163.8:p.Gln1260Pro
ENST00000414678.8:c.3848A>C	ENSP00000412835.3:p.Gln1283Pro
ENST00000637015.2:c.4067A>C	ENSP00000489729.2:p.Gln1356Pro
ENST00000346085.10:c.3818A>C	ENSP00000344546.5:p.Gln1273Pro
ENST00000350026.10:c.3530A>C	ENSP00000055163.7:p.Gln1177Pro
ENST00000414678.7:c.2096A>C	ENSP00000412835.2:p.Gln699Pro
ENST00000635849.1:c.1259A>C	ENSP00000490948.1:p.Gln420Pro
ENST00000635957.1:c.893A>C	ENSP00000490385.1:p.Gln298Pro
ENST00000636930.2:c.3938A>C MANE Select	ENSP00000490491.2:p.Gln1313Pro
ENST00000636940.1:n.1935A>C
ENST00000637015.1:c.1306A>C
ENST00000637568.1:c.1220A>C
ENST00000637741.1:n.604A>C
ENST00000637810.1:c.1280A>C	ENSP00000489636.1:p.Gln427Pro
ENST00000637904.1:c.1439A>C	ENSP00000490550.1:p.Gln480Pro
ENST00000647938.1:c.3569A>C	ENSP00000498155.1:p.Gln1190Pro
ENST00000346085.9:c.3569A>C	ENSP00000344546.4:p.Gln1190Pro
ENST00000350026.9:c.3530A>C	ENSP00000055163.7:p.Gln1177Pro
ENST00000414678.6:c.2096A>C	ENSP00000412835.2:p.Gln699Pro
NM_017519.2:c.3530A>C	NP_059989.2:p.Gln1177Pro
NM_020732.3:c.3569A>C	NP_065783.3:p.Gln1190Pro
XM_005267069.3:c.3689A>C	XP_005267126.2:p.Gln1230Pro
XM_011535984.1:c.2768A>C	XP_011534286.1:p.Gln923Pro
XM_011535985.1:c.2588A>C	XP_011534287.1:p.Gln863Pro
XM_011535986.1:c.2348A>C	XP_011534288.1:p.Gln783Pro
XM_011535987.1:c.1967A>C	XP_011534289.1:p.Gln656Pro
XM_011535988.1:c.830A>C	XP_011534290.1:p.Gln277Pro
NM_001346813.1:c.3689A>C	NP_001333742.1:p.Gln1230Pro
NM_001363725.1:c.1439A>C	NP_001350654.1:p.Gln480Pro
XM_011535984.2:c.3899A>C	XP_011534286.2:p.Gln1300Pro
XM_011535988.3:c.830A>C	XP_011534290.1:p.Gln277Pro
XM_017011103.2:c.3800A>C	XP_016866592.1:p.Gln1267Pro
XM_017011104.1:c.3770A>C	XP_016866593.1:p.Gln1257Pro
XM_017011105.2:c.3740A>C	XP_016866594.1:p.Gln1247Pro
XM_017011106.2:c.3611A>C	XP_016866595.1:p.Gln1204Pro
XM_017011107.2:c.3590A>C	XP_016866596.1:p.Gln1197Pro
XR_002956289.1:n.3982A>C
NM_001363725.2:c.1439A>C	NP_001350654.1:p.Gln480Pro
NM_001371656.1:c.3818A>C	NP_001358585.1:p.Gln1273Pro
NM_001374820.1:c.3818A>C	NP_001361749.1:p.Gln1273Pro
NM_001374828.1:c.3938A>C MANE Select	NP_001361757.1:p.Gln1313Pro
NM_017519.3:c.3779A>C	NP_059989.3:p.Gln1260Pro