Canonical Allele Identifier: CA366239658

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366129
• MyVariant Identifiers: chr6:g.157519977A>C (hg19) ; chr6:g.157198843A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198843A>C , CM000668.2:g.157198843A>C	GRCh38
NC_000006.11:g.157519977A>C , CM000668.1:g.157519977A>C	GRCh37
NC_000006.10:g.157561669A>C	NCBI36
NG_032093.1:g.425914A>C
NG_032093.2:g.425914A>C
NG_066624.1:g.427818A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4256A>C	ENSP00000055163.8:p.Gln1419Pro
ENST00000414678.8:c.4325A>C	ENSP00000412835.3:p.Gln1442Pro
ENST00000637015.2:c.4544A>C	ENSP00000489729.2:p.Gln1515Pro
ENST00000346085.10:c.4295A>C	ENSP00000344546.5:p.Gln1432Pro
ENST00000350026.10:c.4007A>C	ENSP00000055163.7:p.Gln1336Pro
ENST00000414678.7:c.2573A>C	ENSP00000412835.2:p.Gln858Pro
ENST00000635849.1:c.1736A>C	ENSP00000490948.1:p.Gln579Pro
ENST00000635957.1:c.1367A>C	ENSP00000490385.1:p.Gln456Pro
ENST00000636227.1:n.2878A>C
ENST00000636254.1:n.335A>C
ENST00000636930.2:c.4415A>C MANE Select	ENSP00000490491.2:p.Gln1472Pro
ENST00000636940.1:n.2412A>C
ENST00000637015.1:c.1783A>C
ENST00000637568.1:c.1697A>C
ENST00000637741.1:n.1081A>C
ENST00000637810.1:c.1757A>C	ENSP00000489636.1:p.Gln586Pro
ENST00000637904.1:c.1916A>C	ENSP00000490550.1:p.Gln639Pro
ENST00000647938.1:c.4046A>C	ENSP00000498155.1:p.Gln1349Pro
ENST00000346085.9:c.4046A>C	ENSP00000344546.4:p.Gln1349Pro
ENST00000350026.9:c.4007A>C	ENSP00000055163.7:p.Gln1336Pro
ENST00000414678.6:c.2573A>C	ENSP00000412835.2:p.Gln858Pro
NM_017519.2:c.4007A>C	NP_059989.2:p.Gln1336Pro
NM_020732.3:c.4046A>C	NP_065783.3:p.Gln1349Pro
XM_005267069.3:c.4166A>C	XP_005267126.2:p.Gln1389Pro
XM_011535984.1:c.3245A>C	XP_011534286.1:p.Gln1082Pro
XM_011535985.1:c.3065A>C	XP_011534287.1:p.Gln1022Pro
XM_011535986.1:c.2825A>C	XP_011534288.1:p.Gln942Pro
XM_011535987.1:c.2444A>C	XP_011534289.1:p.Gln815Pro
XM_011535988.1:c.1307A>C	XP_011534290.1:p.Gln436Pro
NM_001346813.1:c.4166A>C	NP_001333742.1:p.Gln1389Pro
NM_001363725.1:c.1916A>C	NP_001350654.1:p.Gln639Pro
XM_011535984.2:c.4376A>C	XP_011534286.2:p.Gln1459Pro
XM_011535988.3:c.1307A>C	XP_011534290.1:p.Gln436Pro
XM_017011103.2:c.4277A>C	XP_016866592.1:p.Gln1426Pro
XM_017011104.1:c.4247A>C	XP_016866593.1:p.Gln1416Pro
XM_017011105.2:c.4217A>C	XP_016866594.1:p.Gln1406Pro
XM_017011106.2:c.4088A>C	XP_016866595.1:p.Gln1363Pro
XM_017011107.2:c.4067A>C	XP_016866596.1:p.Gln1356Pro
XR_002956289.1:n.4427-1862A>C
NM_001363725.2:c.1916A>C	NP_001350654.1:p.Gln639Pro
NM_001371656.1:c.4295A>C	NP_001358585.1:p.Gln1432Pro
NM_001374820.1:c.4295A>C	NP_001361749.1:p.Gln1432Pro
NM_001374828.1:c.4415A>C MANE Select	NP_001361757.1:p.Gln1472Pro
NM_017519.3:c.4256A>C	NP_059989.3:p.Gln1419Pro