Canonical Allele Identifier: CA366227822

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231225
• MyVariant Identifiers: chr6:g.157502208G>C (hg19) ; chr6:g.157181074G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181074G>C , CM000668.2:g.157181074G>C	GRCh38
NC_000006.11:g.157502208G>C , CM000668.1:g.157502208G>C	GRCh37
NC_000006.10:g.157543900G>C	NCBI36
NG_032093.1:g.408145G>C
NG_032093.2:g.408145G>C
NG_066624.1:g.410049G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3451G>C	ENSP00000055163.8:p.Glu1151Gln
ENST00000414678.8:c.3520G>C	ENSP00000412835.3:p.Glu1174Gln
ENST00000637015.2:c.3739G>C	ENSP00000489729.2:p.Glu1247Gln
ENST00000319584.11:c.1624G>C	ENSP00000313006.7:p.Glu542Gln
ENST00000346085.10:c.3490G>C	ENSP00000344546.5:p.Glu1164Gln
ENST00000350026.10:c.3202G>C	ENSP00000055163.7:p.Glu1068Gln
ENST00000414678.7:c.1768G>C	ENSP00000412835.2:p.Glu590Gln
ENST00000635849.1:c.931G>C	ENSP00000490948.1:p.Glu311Gln
ENST00000635957.1:c.565G>C	ENSP00000490385.1:p.Glu189Gln
ENST00000636930.2:c.3610G>C MANE Select	ENSP00000490491.2:p.Glu1204Gln
ENST00000636940.1:n.1607G>C
ENST00000637015.1:c.978G>C
ENST00000637568.1:c.892G>C
ENST00000637741.1:n.276G>C
ENST00000637810.1:c.952G>C	ENSP00000489636.1:p.Glu318Gln
ENST00000637904.1:c.1111G>C	ENSP00000490550.1:p.Glu371Gln
ENST00000647938.1:c.3241G>C	ENSP00000498155.1:p.Glu1081Gln
ENST00000319584.10:c.1627G>C	ENSP00000313006.6:p.Glu543Gln
ENST00000346085.9:c.3241G>C	ENSP00000344546.4:p.Glu1081Gln
ENST00000350026.9:c.3202G>C	ENSP00000055163.7:p.Glu1068Gln
ENST00000400790.3:c.403G>C	ENSP00000383596.3:p.Glu135Gln
ENST00000414678.6:c.1768G>C	ENSP00000412835.2:p.Glu590Gln
ENST00000478761.3:c.812G>C
NM_017519.2:c.3202G>C	NP_059989.2:p.Glu1068Gln
NM_020732.3:c.3241G>C	NP_065783.3:p.Glu1081Gln
XM_005267069.3:c.3361G>C	XP_005267126.2:p.Glu1121Gln
XM_011535984.1:c.2440G>C	XP_011534286.1:p.Glu814Gln
XM_011535985.1:c.2260G>C	XP_011534287.1:p.Glu754Gln
XM_011535986.1:c.2020G>C	XP_011534288.1:p.Glu674Gln
XM_011535987.1:c.1639G>C	XP_011534289.1:p.Glu547Gln
XM_011535988.1:c.502G>C	XP_011534290.1:p.Glu168Gln
NM_001346813.1:c.3361G>C	NP_001333742.1:p.Glu1121Gln
NM_001363725.1:c.1111G>C	NP_001350654.1:p.Glu371Gln
XM_011535984.2:c.3571G>C	XP_011534286.2:p.Glu1191Gln
XM_011535988.3:c.502G>C	XP_011534290.1:p.Glu168Gln
XM_017011103.2:c.3472G>C	XP_016866592.1:p.Glu1158Gln
XM_017011104.1:c.3442G>C	XP_016866593.1:p.Glu1148Gln
XM_017011105.2:c.3412G>C	XP_016866594.1:p.Glu1138Gln
XM_017011106.2:c.3283G>C	XP_016866595.1:p.Glu1095Gln
XM_017011107.2:c.3262G>C	XP_016866596.1:p.Glu1088Gln
XR_002956289.1:n.3654G>C
NM_001363725.2:c.1111G>C	NP_001350654.1:p.Glu371Gln
NM_001371656.1:c.3490G>C	NP_001358585.1:p.Glu1164Gln
NM_001374820.1:c.3490G>C	NP_001361749.1:p.Glu1164Gln
NM_001374828.1:c.3610G>C MANE Select	NP_001361757.1:p.Glu1204Gln
NM_017519.3:c.3451G>C	NP_059989.3:p.Glu1151Gln