Canonical Allele Identifier: CA366240883

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521902T>C (hg19) ; chr6:g.157200768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200768T>C , CM000668.2:g.157200768T>C	GRCh38
NC_000006.11:g.157521902T>C , CM000668.1:g.157521902T>C	GRCh37
NC_000006.10:g.157563594T>C	NCBI36
NG_032093.1:g.427839T>C
NG_032093.2:g.427839T>C
NG_066624.1:g.429743T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4384T>C	ENSP00000055163.8:p.Tyr1462His
ENST00000414678.8:c.4453T>C	ENSP00000412835.3:p.Tyr1485His
ENST00000637015.2:c.4672T>C	ENSP00000489729.2:p.Tyr1558His
ENST00000346085.10:c.4423T>C	ENSP00000344546.5:p.Tyr1475His
ENST00000350026.10:c.4135T>C	ENSP00000055163.7:p.Tyr1379His
ENST00000414678.7:c.2701T>C	ENSP00000412835.2:p.Tyr901His
ENST00000635849.1:c.1864T>C	ENSP00000490948.1:p.Tyr622His
ENST00000635957.1:c.1495T>C	ENSP00000490385.1:p.Tyr499His
ENST00000636227.1:n.3006T>C
ENST00000636254.1:n.463T>C
ENST00000636930.2:c.4543T>C MANE Select	ENSP00000490491.2:p.Tyr1515His
ENST00000636940.1:n.2540T>C
ENST00000637015.1:c.1911T>C
ENST00000637568.1:c.1825T>C
ENST00000637741.1:n.1209T>C
ENST00000637810.1:c.1885T>C	ENSP00000489636.1:p.Tyr629His
ENST00000637904.1:c.2044T>C	ENSP00000490550.1:p.Tyr682His
ENST00000647938.1:c.4174T>C	ENSP00000498155.1:p.Tyr1392His
ENST00000346085.9:c.4174T>C	ENSP00000344546.4:p.Tyr1392His
ENST00000350026.9:c.4135T>C	ENSP00000055163.7:p.Tyr1379His
ENST00000414678.6:c.2701T>C	ENSP00000412835.2:p.Tyr901His
NM_017519.2:c.4135T>C	NP_059989.2:p.Tyr1379His
NM_020732.3:c.4174T>C	NP_065783.3:p.Tyr1392His
XM_005267069.3:c.4294T>C	XP_005267126.2:p.Tyr1432His
XM_011535984.1:c.3373T>C	XP_011534286.1:p.Tyr1125His
XM_011535985.1:c.3193T>C	XP_011534287.1:p.Tyr1065His
XM_011535986.1:c.2953T>C	XP_011534288.1:p.Tyr985His
XM_011535987.1:c.2572T>C	XP_011534289.1:p.Tyr858His
XM_011535988.1:c.1435T>C	XP_011534290.1:p.Tyr479His
NM_001346813.1:c.4294T>C	NP_001333742.1:p.Tyr1432His
NM_001363725.1:c.2044T>C	NP_001350654.1:p.Tyr682His
XM_011535984.2:c.4504T>C	XP_011534286.2:p.Tyr1502His
XM_011535988.3:c.1435T>C	XP_011534290.1:p.Tyr479His
XM_017011103.2:c.4405T>C	XP_016866592.1:p.Tyr1469His
XM_017011104.1:c.4375T>C	XP_016866593.1:p.Tyr1459His
XM_017011105.2:c.4345T>C	XP_016866594.1:p.Tyr1449His
XM_017011106.2:c.4216T>C	XP_016866595.1:p.Tyr1406His
XM_017011107.2:c.4195T>C	XP_016866596.1:p.Tyr1399His
XR_002956289.1:n.4490T>C
NM_001363725.2:c.2044T>C	NP_001350654.1:p.Tyr682His
NM_001371656.1:c.4423T>C	NP_001358585.1:p.Tyr1475His
NM_001374820.1:c.4423T>C	NP_001361749.1:p.Tyr1475His
NM_001374828.1:c.4543T>C MANE Select	NP_001361757.1:p.Tyr1515His
NM_017519.3:c.4384T>C	NP_059989.3:p.Tyr1462His