Canonical Allele Identifier: CA366241486

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201011-T-C
• MyVariant Identifiers: chr6:g.157522145T>C (hg19) ; chr6:g.157201011T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201011T>C , CM000668.2:g.157201011T>C	GRCh38
NC_000006.11:g.157522145T>C , CM000668.1:g.157522145T>C	GRCh37
NC_000006.10:g.157563837T>C	NCBI36
NG_032093.1:g.428082T>C
NG_032093.2:g.428082T>C
NG_066624.1:g.429986T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4627T>C	ENSP00000055163.8:p.Tyr1543His
ENST00000414678.8:c.4696T>C	ENSP00000412835.3:p.Tyr1566His
ENST00000637015.2:c.4915T>C	ENSP00000489729.2:p.Tyr1639His
ENST00000346085.10:c.4666T>C	ENSP00000344546.5:p.Tyr1556His
ENST00000350026.10:c.4378T>C	ENSP00000055163.7:p.Tyr1460His
ENST00000414678.7:c.2944T>C	ENSP00000412835.2:p.Tyr982His
ENST00000635849.1:c.2107T>C	ENSP00000490948.1:p.Tyr703His
ENST00000635957.1:c.1738T>C	ENSP00000490385.1:p.Tyr580His
ENST00000636227.1:n.3249T>C
ENST00000636254.1:n.706T>C
ENST00000636930.2:c.4786T>C MANE Select	ENSP00000490491.2:p.Tyr1596His
ENST00000636940.1:n.2783T>C
ENST00000637015.1:c.2154T>C
ENST00000637568.1:c.2068T>C
ENST00000637741.1:n.1452T>C
ENST00000637810.1:c.2128T>C	ENSP00000489636.1:p.Tyr710His
ENST00000637904.1:c.2287T>C	ENSP00000490550.1:p.Tyr763His
ENST00000647938.1:c.4417T>C	ENSP00000498155.1:p.Tyr1473His
ENST00000346085.9:c.4417T>C	ENSP00000344546.4:p.Tyr1473His
ENST00000350026.9:c.4378T>C	ENSP00000055163.7:p.Tyr1460His
ENST00000414678.6:c.2944T>C	ENSP00000412835.2:p.Tyr982His
NM_017519.2:c.4378T>C	NP_059989.2:p.Tyr1460His
NM_020732.3:c.4417T>C	NP_065783.3:p.Tyr1473His
XM_005267069.3:c.4537T>C	XP_005267126.2:p.Tyr1513His
XM_011535984.1:c.3616T>C	XP_011534286.1:p.Tyr1206His
XM_011535985.1:c.3436T>C	XP_011534287.1:p.Tyr1146His
XM_011535986.1:c.3196T>C	XP_011534288.1:p.Tyr1066His
XM_011535987.1:c.2815T>C	XP_011534289.1:p.Tyr939His
XM_011535988.1:c.1678T>C	XP_011534290.1:p.Tyr560His
NM_001346813.1:c.4537T>C	NP_001333742.1:p.Tyr1513His
NM_001363725.1:c.2287T>C	NP_001350654.1:p.Tyr763His
XM_011535984.2:c.4747T>C	XP_011534286.2:p.Tyr1583His
XM_011535988.3:c.1678T>C	XP_011534290.1:p.Tyr560His
XM_017011103.2:c.4648T>C	XP_016866592.1:p.Tyr1550His
XM_017011104.1:c.4618T>C	XP_016866593.1:p.Tyr1540His
XM_017011105.2:c.4588T>C	XP_016866594.1:p.Tyr1530His
XM_017011106.2:c.4459T>C	XP_016866595.1:p.Tyr1487His
XM_017011107.2:c.4438T>C	XP_016866596.1:p.Tyr1480His
XR_002956289.1:n.4733T>C
NM_001363725.2:c.2287T>C	NP_001350654.1:p.Tyr763His
NM_001371656.1:c.4666T>C	NP_001358585.1:p.Tyr1556His
NM_001374820.1:c.4666T>C	NP_001361749.1:p.Tyr1556His
NM_001374828.1:c.4786T>C MANE Select	NP_001361757.1:p.Tyr1596His
NM_017519.3:c.4627T>C	NP_059989.3:p.Tyr1543His