Canonical Allele Identifier: CA366242767

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376289
• MyVariant Identifiers: chr6:g.157522501G>C (hg19) ; chr6:g.157201367G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201367G>C , CM000668.2:g.157201367G>C	GRCh38
NC_000006.11:g.157522501G>C , CM000668.1:g.157522501G>C	GRCh37
NC_000006.10:g.157564193G>C	NCBI36
NG_032093.1:g.428438G>C
NG_032093.2:g.428438G>C
NG_066624.1:g.430342G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4983G>C	ENSP00000055163.8:p.Gln1661His
ENST00000414678.8:c.5052G>C	ENSP00000412835.3:p.Gln1684His
ENST00000637015.2:c.5271G>C	ENSP00000489729.2:p.Gln1757His
ENST00000346085.10:c.5022G>C	ENSP00000344546.5:p.Gln1674His
ENST00000350026.10:c.4734G>C	ENSP00000055163.7:p.Gln1578His
ENST00000414678.7:c.3300G>C	ENSP00000412835.2:p.Gln1100His
ENST00000635849.1:c.2463G>C	ENSP00000490948.1:p.Gln821His
ENST00000635957.1:c.2094G>C	ENSP00000490385.1:p.Gln698His
ENST00000636227.1:n.3605G>C
ENST00000636254.1:n.1062G>C
ENST00000636930.2:c.5142G>C MANE Select	ENSP00000490491.2:p.Gln1714His
ENST00000636940.1:n.3139G>C
ENST00000637015.1:c.2510G>C
ENST00000637568.1:c.2424G>C
ENST00000637741.1:n.1808G>C
ENST00000637810.1:c.2484G>C	ENSP00000489636.1:p.Gln828His
ENST00000637904.1:c.2643G>C	ENSP00000490550.1:p.Gln881His
ENST00000647938.1:c.4773G>C	ENSP00000498155.1:p.Gln1591His
ENST00000346085.9:c.4773G>C	ENSP00000344546.4:p.Gln1591His
ENST00000350026.9:c.4734G>C	ENSP00000055163.7:p.Gln1578His
ENST00000414678.6:c.3300G>C	ENSP00000412835.2:p.Gln1100His
NM_017519.2:c.4734G>C	NP_059989.2:p.Gln1578His
NM_020732.3:c.4773G>C	NP_065783.3:p.Gln1591His
XM_005267069.3:c.4893G>C	XP_005267126.2:p.Gln1631His
XM_011535984.1:c.3972G>C	XP_011534286.1:p.Gln1324His
XM_011535985.1:c.3792G>C	XP_011534287.1:p.Gln1264His
XM_011535986.1:c.3552G>C	XP_011534288.1:p.Gln1184His
XM_011535987.1:c.3171G>C	XP_011534289.1:p.Gln1057His
XM_011535988.1:c.2034G>C	XP_011534290.1:p.Gln678His
NM_001346813.1:c.4893G>C	NP_001333742.1:p.Gln1631His
NM_001363725.1:c.2643G>C	NP_001350654.1:p.Gln881His
XM_011535984.2:c.5103G>C	XP_011534286.2:p.Gln1701His
XM_011535988.3:c.2034G>C	XP_011534290.1:p.Gln678His
XM_017011103.2:c.5004G>C	XP_016866592.1:p.Gln1668His
XM_017011104.1:c.4974G>C	XP_016866593.1:p.Gln1658His
XM_017011105.2:c.4944G>C	XP_016866594.1:p.Gln1648His
XM_017011106.2:c.4815G>C	XP_016866595.1:p.Gln1605His
XM_017011107.2:c.4794G>C	XP_016866596.1:p.Gln1598His
XR_002956289.1:n.5089G>C
NM_001363725.2:c.2643G>C	NP_001350654.1:p.Gln881His
NM_001371656.1:c.5022G>C	NP_001358585.1:p.Gln1674His
NM_001374820.1:c.5022G>C	NP_001361749.1:p.Gln1674His
NM_001374828.1:c.5142G>C MANE Select	NP_001361757.1:p.Gln1714His
NM_017519.3:c.4983G>C	NP_059989.3:p.Gln1661His