Canonical Allele Identifier: CA366227160

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502131A>C (hg19) ; chr6:g.157180997A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157180997A>C , CM000668.2:g.157180997A>C	GRCh38
NC_000006.11:g.157502131A>C , CM000668.1:g.157502131A>C	GRCh37
NC_000006.10:g.157543823A>C	NCBI36
NG_032093.1:g.408068A>C
NG_032093.2:g.408068A>C
NG_066624.1:g.409972A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3374A>C	ENSP00000055163.8:p.Glu1125Ala
ENST00000414678.8:c.3443A>C	ENSP00000412835.3:p.Glu1148Ala
ENST00000637015.2:c.3662A>C	ENSP00000489729.2:p.Glu1221Ala
ENST00000319584.11:c.1547A>C	ENSP00000313006.7:p.Glu516Ala
ENST00000346085.10:c.3413A>C	ENSP00000344546.5:p.Glu1138Ala
ENST00000350026.10:c.3125A>C	ENSP00000055163.7:p.Glu1042Ala
ENST00000414678.7:c.1691A>C	ENSP00000412835.2:p.Glu564Ala
ENST00000635849.1:c.854A>C	ENSP00000490948.1:p.Glu285Ala
ENST00000635957.1:c.488A>C	ENSP00000490385.1:p.Glu163Ala
ENST00000636930.2:c.3533A>C MANE Select	ENSP00000490491.2:p.Glu1178Ala
ENST00000636940.1:n.1530A>C
ENST00000637015.1:c.901A>C
ENST00000637568.1:c.815A>C
ENST00000637741.1:n.199A>C
ENST00000637810.1:c.875A>C	ENSP00000489636.1:p.Glu292Ala
ENST00000637904.1:c.1034A>C	ENSP00000490550.1:p.Glu345Ala
ENST00000647938.1:c.3164A>C	ENSP00000498155.1:p.Glu1055Ala
ENST00000319584.10:c.1550A>C	ENSP00000313006.6:p.Glu517Ala
ENST00000346085.9:c.3164A>C	ENSP00000344546.4:p.Glu1055Ala
ENST00000350026.9:c.3125A>C	ENSP00000055163.7:p.Glu1042Ala
ENST00000400790.3:c.326A>C	ENSP00000383596.3:p.Glu109Ala
ENST00000414678.6:c.1691A>C	ENSP00000412835.2:p.Glu564Ala
ENST00000478761.3:c.735A>C
NM_017519.2:c.3125A>C	NP_059989.2:p.Glu1042Ala
NM_020732.3:c.3164A>C	NP_065783.3:p.Glu1055Ala
XM_005267069.3:c.3284A>C	XP_005267126.2:p.Glu1095Ala
XM_011535984.1:c.2363A>C	XP_011534286.1:p.Glu788Ala
XM_011535985.1:c.2183A>C	XP_011534287.1:p.Glu728Ala
XM_011535986.1:c.1943A>C	XP_011534288.1:p.Glu648Ala
XM_011535987.1:c.1562A>C	XP_011534289.1:p.Glu521Ala
XM_011535988.1:c.425A>C	XP_011534290.1:p.Glu142Ala
NM_001346813.1:c.3284A>C	NP_001333742.1:p.Glu1095Ala
NM_001363725.1:c.1034A>C	NP_001350654.1:p.Glu345Ala
XM_011535984.2:c.3494A>C	XP_011534286.2:p.Glu1165Ala
XM_011535988.3:c.425A>C	XP_011534290.1:p.Glu142Ala
XM_017011103.2:c.3395A>C	XP_016866592.1:p.Glu1132Ala
XM_017011104.1:c.3365A>C	XP_016866593.1:p.Glu1122Ala
XM_017011105.2:c.3335A>C	XP_016866594.1:p.Glu1112Ala
XM_017011106.2:c.3206A>C	XP_016866595.1:p.Glu1069Ala
XM_017011107.2:c.3185A>C	XP_016866596.1:p.Glu1062Ala
XR_002956289.1:n.3577A>C
NM_001363725.2:c.1034A>C	NP_001350654.1:p.Glu345Ala
NM_001371656.1:c.3413A>C	NP_001358585.1:p.Glu1138Ala
NM_001374820.1:c.3413A>C	NP_001361749.1:p.Glu1138Ala
NM_001374828.1:c.3533A>C MANE Select	NP_001361757.1:p.Glu1178Ala
NM_017519.3:c.3374A>C	NP_059989.3:p.Glu1125Ala