Canonical Allele Identifier: CA366234190

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338974
• gnomAD v4: 6-157189737-G-A
• MyVariant Identifiers: chr6:g.157510871G>A (hg19) ; chr6:g.157189737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189737G>A , CM000668.2:g.157189737G>A	GRCh38
NC_000006.11:g.157510871G>A , CM000668.1:g.157510871G>A	GRCh37
NC_000006.10:g.157552563G>A	NCBI36
NG_032093.1:g.416808G>A
NG_032093.2:g.416808G>A
NG_066624.1:g.418712G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3856G>A	ENSP00000055163.8:p.Ala1286Thr
ENST00000414678.8:c.3925G>A	ENSP00000412835.3:p.Ala1309Thr
ENST00000637015.2:c.4144G>A	ENSP00000489729.2:p.Ala1382Thr
ENST00000346085.10:c.3895G>A	ENSP00000344546.5:p.Ala1299Thr
ENST00000350026.10:c.3607G>A	ENSP00000055163.7:p.Ala1203Thr
ENST00000414678.7:c.2173G>A	ENSP00000412835.2:p.Ala725Thr
ENST00000635849.1:c.1336G>A	ENSP00000490948.1:p.Ala446Thr
ENST00000635957.1:c.970G>A	ENSP00000490385.1:p.Ala324Thr
ENST00000636930.2:c.4015G>A MANE Select	ENSP00000490491.2:p.Ala1339Thr
ENST00000636940.1:n.2012G>A
ENST00000637015.1:c.1383G>A
ENST00000637568.1:c.1297G>A
ENST00000637741.1:n.681G>A
ENST00000637810.1:c.1357G>A	ENSP00000489636.1:p.Ala453Thr
ENST00000637904.1:c.1516G>A	ENSP00000490550.1:p.Ala506Thr
ENST00000647938.1:c.3646G>A	ENSP00000498155.1:p.Ala1216Thr
ENST00000346085.9:c.3646G>A	ENSP00000344546.4:p.Ala1216Thr
ENST00000350026.9:c.3607G>A	ENSP00000055163.7:p.Ala1203Thr
ENST00000414678.6:c.2173G>A	ENSP00000412835.2:p.Ala725Thr
NM_017519.2:c.3607G>A	NP_059989.2:p.Ala1203Thr
NM_020732.3:c.3646G>A	NP_065783.3:p.Ala1216Thr
XM_005267069.3:c.3766G>A	XP_005267126.2:p.Ala1256Thr
XM_011535984.1:c.2845G>A	XP_011534286.1:p.Ala949Thr
XM_011535985.1:c.2665G>A	XP_011534287.1:p.Ala889Thr
XM_011535986.1:c.2425G>A	XP_011534288.1:p.Ala809Thr
XM_011535987.1:c.2044G>A	XP_011534289.1:p.Ala682Thr
XM_011535988.1:c.907G>A	XP_011534290.1:p.Ala303Thr
NM_001346813.1:c.3766G>A	NP_001333742.1:p.Ala1256Thr
NM_001363725.1:c.1516G>A	NP_001350654.1:p.Ala506Thr
XM_011535984.2:c.3976G>A	XP_011534286.2:p.Ala1326Thr
XM_011535988.3:c.907G>A	XP_011534290.1:p.Ala303Thr
XM_017011103.2:c.3877G>A	XP_016866592.1:p.Ala1293Thr
XM_017011104.1:c.3847G>A	XP_016866593.1:p.Ala1283Thr
XM_017011105.2:c.3817G>A	XP_016866594.1:p.Ala1273Thr
XM_017011106.2:c.3688G>A	XP_016866595.1:p.Ala1230Thr
XM_017011107.2:c.3667G>A	XP_016866596.1:p.Ala1223Thr
XR_002956289.1:n.4059G>A
NM_001363725.2:c.1516G>A	NP_001350654.1:p.Ala506Thr
NM_001371656.1:c.3895G>A	NP_001358585.1:p.Ala1299Thr
NM_001374820.1:c.3895G>A	NP_001361749.1:p.Ala1299Thr
NM_001374828.1:c.4015G>A MANE Select	NP_001361757.1:p.Ala1339Thr
NM_017519.3:c.3856G>A	NP_059989.3:p.Ala1286Thr