Canonical Allele Identifier: CA366241912

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522221A>C (hg19) ; chr6:g.157201087A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201087A>C , CM000668.2:g.157201087A>C	GRCh38
NC_000006.11:g.157522221A>C , CM000668.1:g.157522221A>C	GRCh37
NC_000006.10:g.157563913A>C	NCBI36
NG_032093.1:g.428158A>C
NG_032093.2:g.428158A>C
NG_066624.1:g.430062A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4703A>C	ENSP00000055163.8:p.Asp1568Ala
ENST00000414678.8:c.4772A>C	ENSP00000412835.3:p.Asp1591Ala
ENST00000637015.2:c.4991A>C	ENSP00000489729.2:p.Asp1664Ala
ENST00000346085.10:c.4742A>C	ENSP00000344546.5:p.Asp1581Ala
ENST00000350026.10:c.4454A>C	ENSP00000055163.7:p.Asp1485Ala
ENST00000414678.7:c.3020A>C	ENSP00000412835.2:p.Asp1007Ala
ENST00000635849.1:c.2183A>C	ENSP00000490948.1:p.Asp728Ala
ENST00000635957.1:c.1814A>C	ENSP00000490385.1:p.Asp605Ala
ENST00000636227.1:n.3325A>C
ENST00000636254.1:n.782A>C
ENST00000636930.2:c.4862A>C MANE Select	ENSP00000490491.2:p.Asp1621Ala
ENST00000636940.1:n.2859A>C
ENST00000637015.1:c.2230A>C
ENST00000637568.1:c.2144A>C
ENST00000637741.1:n.1528A>C
ENST00000637810.1:c.2204A>C	ENSP00000489636.1:p.Asp735Ala
ENST00000637904.1:c.2363A>C	ENSP00000490550.1:p.Asp788Ala
ENST00000647938.1:c.4493A>C	ENSP00000498155.1:p.Asp1498Ala
ENST00000346085.9:c.4493A>C	ENSP00000344546.4:p.Asp1498Ala
ENST00000350026.9:c.4454A>C	ENSP00000055163.7:p.Asp1485Ala
ENST00000414678.6:c.3020A>C	ENSP00000412835.2:p.Asp1007Ala
NM_017519.2:c.4454A>C	NP_059989.2:p.Asp1485Ala
NM_020732.3:c.4493A>C	NP_065783.3:p.Asp1498Ala
XM_005267069.3:c.4613A>C	XP_005267126.2:p.Asp1538Ala
XM_011535984.1:c.3692A>C	XP_011534286.1:p.Asp1231Ala
XM_011535985.1:c.3512A>C	XP_011534287.1:p.Asp1171Ala
XM_011535986.1:c.3272A>C	XP_011534288.1:p.Asp1091Ala
XM_011535987.1:c.2891A>C	XP_011534289.1:p.Asp964Ala
XM_011535988.1:c.1754A>C	XP_011534290.1:p.Asp585Ala
NM_001346813.1:c.4613A>C	NP_001333742.1:p.Asp1538Ala
NM_001363725.1:c.2363A>C	NP_001350654.1:p.Asp788Ala
XM_011535984.2:c.4823A>C	XP_011534286.2:p.Asp1608Ala
XM_011535988.3:c.1754A>C	XP_011534290.1:p.Asp585Ala
XM_017011103.2:c.4724A>C	XP_016866592.1:p.Asp1575Ala
XM_017011104.1:c.4694A>C	XP_016866593.1:p.Asp1565Ala
XM_017011105.2:c.4664A>C	XP_016866594.1:p.Asp1555Ala
XM_017011106.2:c.4535A>C	XP_016866595.1:p.Asp1512Ala
XM_017011107.2:c.4514A>C	XP_016866596.1:p.Asp1505Ala
XR_002956289.1:n.4809A>C
NM_001363725.2:c.2363A>C	NP_001350654.1:p.Asp788Ala
NM_001371656.1:c.4742A>C	NP_001358585.1:p.Asp1581Ala
NM_001374820.1:c.4742A>C	NP_001361749.1:p.Asp1581Ala
NM_001374828.1:c.4862A>C MANE Select	NP_001361757.1:p.Asp1621Ala
NM_017519.3:c.4703A>C	NP_059989.3:p.Asp1568Ala