Canonical Allele Identifier: CA366235324

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511260T>C (hg19) ; chr6:g.157190126T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190126T>C , CM000668.2:g.157190126T>C	GRCh38
NC_000006.11:g.157511260T>C , CM000668.1:g.157511260T>C	GRCh37
NC_000006.10:g.157552952T>C	NCBI36
NG_032093.1:g.417197T>C
NG_032093.2:g.417197T>C
NG_066624.1:g.419101T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3988T>C	ENSP00000055163.8:p.Tyr1330His
ENST00000414678.8:c.4057T>C	ENSP00000412835.3:p.Tyr1353His
ENST00000637015.2:c.4276T>C	ENSP00000489729.2:p.Tyr1426His
ENST00000346085.10:c.4027T>C	ENSP00000344546.5:p.Tyr1343His
ENST00000350026.10:c.3739T>C	ENSP00000055163.7:p.Tyr1247His
ENST00000414678.7:c.2305T>C	ENSP00000412835.2:p.Tyr769His
ENST00000635849.1:c.1468T>C	ENSP00000490948.1:p.Tyr490His
ENST00000635957.1:c.1099T>C	ENSP00000490385.1:p.Tyr367His
ENST00000636930.2:c.4147T>C MANE Select	ENSP00000490491.2:p.Tyr1383His
ENST00000636940.1:n.2144T>C
ENST00000637015.1:c.1515T>C
ENST00000637568.1:c.1429T>C
ENST00000637741.1:n.813T>C
ENST00000637810.1:c.1489T>C	ENSP00000489636.1:p.Tyr497His
ENST00000637904.1:c.1648T>C	ENSP00000490550.1:p.Tyr550His
ENST00000647938.1:c.3778T>C	ENSP00000498155.1:p.Tyr1260His
ENST00000346085.9:c.3778T>C	ENSP00000344546.4:p.Tyr1260His
ENST00000350026.9:c.3739T>C	ENSP00000055163.7:p.Tyr1247His
ENST00000414678.6:c.2305T>C	ENSP00000412835.2:p.Tyr769His
NM_017519.2:c.3739T>C	NP_059989.2:p.Tyr1247His
NM_020732.3:c.3778T>C	NP_065783.3:p.Tyr1260His
XM_005267069.3:c.3898T>C	XP_005267126.2:p.Tyr1300His
XM_011535984.1:c.2977T>C	XP_011534286.1:p.Tyr993His
XM_011535985.1:c.2797T>C	XP_011534287.1:p.Tyr933His
XM_011535986.1:c.2557T>C	XP_011534288.1:p.Tyr853His
XM_011535987.1:c.2176T>C	XP_011534289.1:p.Tyr726His
XM_011535988.1:c.1039T>C	XP_011534290.1:p.Tyr347His
NM_001346813.1:c.3898T>C	NP_001333742.1:p.Tyr1300His
NM_001363725.1:c.1648T>C	NP_001350654.1:p.Tyr550His
XM_011535984.2:c.4108T>C	XP_011534286.2:p.Tyr1370His
XM_011535988.3:c.1039T>C	XP_011534290.1:p.Tyr347His
XM_017011103.2:c.4009T>C	XP_016866592.1:p.Tyr1337His
XM_017011104.1:c.3979T>C	XP_016866593.1:p.Tyr1327His
XM_017011105.2:c.3949T>C	XP_016866594.1:p.Tyr1317His
XM_017011106.2:c.3820T>C	XP_016866595.1:p.Tyr1274His
XM_017011107.2:c.3799T>C	XP_016866596.1:p.Tyr1267His
XR_002956289.1:n.4191T>C
NM_001363725.2:c.1648T>C	NP_001350654.1:p.Tyr550His
NM_001371656.1:c.4027T>C	NP_001358585.1:p.Tyr1343His
NM_001374820.1:c.4027T>C	NP_001361749.1:p.Tyr1343His
NM_001374828.1:c.4147T>C MANE Select	NP_001361757.1:p.Tyr1383His
NM_017519.3:c.3988T>C	NP_059989.3:p.Tyr1330His