Canonical Allele Identifier: CA366234674

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511182A>C (hg19) ; chr6:g.157190048A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190048A>C , CM000668.2:g.157190048A>C	GRCh38
NC_000006.11:g.157511182A>C , CM000668.1:g.157511182A>C	GRCh37
NC_000006.10:g.157552874A>C	NCBI36
NG_032093.1:g.417119A>C
NG_032093.2:g.417119A>C
NG_066624.1:g.419023A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3910A>C	ENSP00000055163.8:p.Ile1304Leu
ENST00000414678.8:c.3979A>C	ENSP00000412835.3:p.Ile1327Leu
ENST00000637015.2:c.4198A>C	ENSP00000489729.2:p.Ile1400Leu
ENST00000346085.10:c.3949A>C	ENSP00000344546.5:p.Ile1317Leu
ENST00000350026.10:c.3661A>C	ENSP00000055163.7:p.Ile1221Leu
ENST00000414678.7:c.2227A>C	ENSP00000412835.2:p.Ile743Leu
ENST00000635849.1:c.1390A>C	ENSP00000490948.1:p.Ile464Leu
ENST00000635957.1:c.1021A>C	ENSP00000490385.1:p.Ile341Leu
ENST00000636930.2:c.4069A>C MANE Select	ENSP00000490491.2:p.Ile1357Leu
ENST00000636940.1:n.2066A>C
ENST00000637015.1:c.1437A>C
ENST00000637568.1:c.1351A>C
ENST00000637741.1:n.735A>C
ENST00000637810.1:c.1411A>C	ENSP00000489636.1:p.Ile471Leu
ENST00000637904.1:c.1570A>C	ENSP00000490550.1:p.Ile524Leu
ENST00000647938.1:c.3700A>C	ENSP00000498155.1:p.Ile1234Leu
ENST00000346085.9:c.3700A>C	ENSP00000344546.4:p.Ile1234Leu
ENST00000350026.9:c.3661A>C	ENSP00000055163.7:p.Ile1221Leu
ENST00000414678.6:c.2227A>C	ENSP00000412835.2:p.Ile743Leu
NM_017519.2:c.3661A>C	NP_059989.2:p.Ile1221Leu
NM_020732.3:c.3700A>C	NP_065783.3:p.Ile1234Leu
XM_005267069.3:c.3820A>C	XP_005267126.2:p.Ile1274Leu
XM_011535984.1:c.2899A>C	XP_011534286.1:p.Ile967Leu
XM_011535985.1:c.2719A>C	XP_011534287.1:p.Ile907Leu
XM_011535986.1:c.2479A>C	XP_011534288.1:p.Ile827Leu
XM_011535987.1:c.2098A>C	XP_011534289.1:p.Ile700Leu
XM_011535988.1:c.961A>C	XP_011534290.1:p.Ile321Leu
NM_001346813.1:c.3820A>C	NP_001333742.1:p.Ile1274Leu
NM_001363725.1:c.1570A>C	NP_001350654.1:p.Ile524Leu
XM_011535984.2:c.4030A>C	XP_011534286.2:p.Ile1344Leu
XM_011535988.3:c.961A>C	XP_011534290.1:p.Ile321Leu
XM_017011103.2:c.3931A>C	XP_016866592.1:p.Ile1311Leu
XM_017011104.1:c.3901A>C	XP_016866593.1:p.Ile1301Leu
XM_017011105.2:c.3871A>C	XP_016866594.1:p.Ile1291Leu
XM_017011106.2:c.3742A>C	XP_016866595.1:p.Ile1248Leu
XM_017011107.2:c.3721A>C	XP_016866596.1:p.Ile1241Leu
XR_002956289.1:n.4113A>C
NM_001363725.2:c.1570A>C	NP_001350654.1:p.Ile524Leu
NM_001371656.1:c.3949A>C	NP_001358585.1:p.Ile1317Leu
NM_001374820.1:c.3949A>C	NP_001361749.1:p.Ile1317Leu
NM_001374828.1:c.4069A>C MANE Select	NP_001361757.1:p.Ile1357Leu
NM_017519.3:c.3910A>C	NP_059989.3:p.Ile1304Leu