Canonical Allele Identifier: CA366242382

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201274-G-C
• MyVariant Identifiers: chr6:g.157522408G>C (hg19) ; chr6:g.157201274G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201274G>C , CM000668.2:g.157201274G>C	GRCh38
NC_000006.11:g.157522408G>C , CM000668.1:g.157522408G>C	GRCh37
NC_000006.10:g.157564100G>C	NCBI36
NG_032093.1:g.428345G>C
NG_032093.2:g.428345G>C
NG_066624.1:g.430249G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4890G>C	ENSP00000055163.8:p.Gln1630His
ENST00000414678.8:c.4959G>C	ENSP00000412835.3:p.Gln1653His
ENST00000637015.2:c.5178G>C	ENSP00000489729.2:p.Gln1726His
ENST00000346085.10:c.4929G>C	ENSP00000344546.5:p.Gln1643His
ENST00000350026.10:c.4641G>C	ENSP00000055163.7:p.Gln1547His
ENST00000414678.7:c.3207G>C	ENSP00000412835.2:p.Gln1069His
ENST00000635849.1:c.2370G>C	ENSP00000490948.1:p.Gln790His
ENST00000635957.1:c.2001G>C	ENSP00000490385.1:p.Gln667His
ENST00000636227.1:n.3512G>C
ENST00000636254.1:n.969G>C
ENST00000636930.2:c.5049G>C MANE Select	ENSP00000490491.2:p.Gln1683His
ENST00000636940.1:n.3046G>C
ENST00000637015.1:c.2417G>C
ENST00000637568.1:c.2331G>C
ENST00000637741.1:n.1715G>C
ENST00000637810.1:c.2391G>C	ENSP00000489636.1:p.Gln797His
ENST00000637904.1:c.2550G>C	ENSP00000490550.1:p.Gln850His
ENST00000647938.1:c.4680G>C	ENSP00000498155.1:p.Gln1560His
ENST00000346085.9:c.4680G>C	ENSP00000344546.4:p.Gln1560His
ENST00000350026.9:c.4641G>C	ENSP00000055163.7:p.Gln1547His
ENST00000414678.6:c.3207G>C	ENSP00000412835.2:p.Gln1069His
NM_017519.2:c.4641G>C	NP_059989.2:p.Gln1547His
NM_020732.3:c.4680G>C	NP_065783.3:p.Gln1560His
XM_005267069.3:c.4800G>C	XP_005267126.2:p.Gln1600His
XM_011535984.1:c.3879G>C	XP_011534286.1:p.Gln1293His
XM_011535985.1:c.3699G>C	XP_011534287.1:p.Gln1233His
XM_011535986.1:c.3459G>C	XP_011534288.1:p.Gln1153His
XM_011535987.1:c.3078G>C	XP_011534289.1:p.Gln1026His
XM_011535988.1:c.1941G>C	XP_011534290.1:p.Gln647His
NM_001346813.1:c.4800G>C	NP_001333742.1:p.Gln1600His
NM_001363725.1:c.2550G>C	NP_001350654.1:p.Gln850His
XM_011535984.2:c.5010G>C	XP_011534286.2:p.Gln1670His
XM_011535988.3:c.1941G>C	XP_011534290.1:p.Gln647His
XM_017011103.2:c.4911G>C	XP_016866592.1:p.Gln1637His
XM_017011104.1:c.4881G>C	XP_016866593.1:p.Gln1627His
XM_017011105.2:c.4851G>C	XP_016866594.1:p.Gln1617His
XM_017011106.2:c.4722G>C	XP_016866595.1:p.Gln1574His
XM_017011107.2:c.4701G>C	XP_016866596.1:p.Gln1567His
XR_002956289.1:n.4996G>C
NM_001363725.2:c.2550G>C	NP_001350654.1:p.Gln850His
NM_001371656.1:c.4929G>C	NP_001358585.1:p.Gln1643His
NM_001374820.1:c.4929G>C	NP_001361749.1:p.Gln1643His
NM_001374828.1:c.5049G>C MANE Select	NP_001361757.1:p.Gln1683His
NM_017519.3:c.4890G>C	NP_059989.3:p.Gln1630His