Canonical Allele Identifier: CA366234969

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511210T>C (hg19) ; chr6:g.157190076T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190076T>C , CM000668.2:g.157190076T>C	GRCh38
NC_000006.11:g.157511210T>C , CM000668.1:g.157511210T>C	GRCh37
NC_000006.10:g.157552902T>C	NCBI36
NG_032093.1:g.417147T>C
NG_032093.2:g.417147T>C
NG_066624.1:g.419051T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3938T>C	ENSP00000055163.8:p.Val1313Ala
ENST00000414678.8:c.4007T>C	ENSP00000412835.3:p.Val1336Ala
ENST00000637015.2:c.4226T>C	ENSP00000489729.2:p.Val1409Ala
ENST00000346085.10:c.3977T>C	ENSP00000344546.5:p.Val1326Ala
ENST00000350026.10:c.3689T>C	ENSP00000055163.7:p.Val1230Ala
ENST00000414678.7:c.2255T>C	ENSP00000412835.2:p.Val752Ala
ENST00000635849.1:c.1418T>C	ENSP00000490948.1:p.Val473Ala
ENST00000635957.1:c.1049T>C	ENSP00000490385.1:p.Val350Ala
ENST00000636930.2:c.4097T>C MANE Select	ENSP00000490491.2:p.Val1366Ala
ENST00000636940.1:n.2094T>C
ENST00000637015.1:c.1465T>C
ENST00000637568.1:c.1379T>C
ENST00000637741.1:n.763T>C
ENST00000637810.1:c.1439T>C	ENSP00000489636.1:p.Val480Ala
ENST00000637904.1:c.1598T>C	ENSP00000490550.1:p.Val533Ala
ENST00000647938.1:c.3728T>C	ENSP00000498155.1:p.Val1243Ala
ENST00000346085.9:c.3728T>C	ENSP00000344546.4:p.Val1243Ala
ENST00000350026.9:c.3689T>C	ENSP00000055163.7:p.Val1230Ala
ENST00000414678.6:c.2255T>C	ENSP00000412835.2:p.Val752Ala
NM_017519.2:c.3689T>C	NP_059989.2:p.Val1230Ala
NM_020732.3:c.3728T>C	NP_065783.3:p.Val1243Ala
XM_005267069.3:c.3848T>C	XP_005267126.2:p.Val1283Ala
XM_011535984.1:c.2927T>C	XP_011534286.1:p.Val976Ala
XM_011535985.1:c.2747T>C	XP_011534287.1:p.Val916Ala
XM_011535986.1:c.2507T>C	XP_011534288.1:p.Val836Ala
XM_011535987.1:c.2126T>C	XP_011534289.1:p.Val709Ala
XM_011535988.1:c.989T>C	XP_011534290.1:p.Val330Ala
NM_001346813.1:c.3848T>C	NP_001333742.1:p.Val1283Ala
NM_001363725.1:c.1598T>C	NP_001350654.1:p.Val533Ala
XM_011535984.2:c.4058T>C	XP_011534286.2:p.Val1353Ala
XM_011535988.3:c.989T>C	XP_011534290.1:p.Val330Ala
XM_017011103.2:c.3959T>C	XP_016866592.1:p.Val1320Ala
XM_017011104.1:c.3929T>C	XP_016866593.1:p.Val1310Ala
XM_017011105.2:c.3899T>C	XP_016866594.1:p.Val1300Ala
XM_017011106.2:c.3770T>C	XP_016866595.1:p.Val1257Ala
XM_017011107.2:c.3749T>C	XP_016866596.1:p.Val1250Ala
XR_002956289.1:n.4141T>C
NM_001363725.2:c.1598T>C	NP_001350654.1:p.Val533Ala
NM_001371656.1:c.3977T>C	NP_001358585.1:p.Val1326Ala
NM_001374820.1:c.3977T>C	NP_001361749.1:p.Val1326Ala
NM_001374828.1:c.4097T>C MANE Select	NP_001361757.1:p.Val1366Ala
NM_017519.3:c.3938T>C	NP_059989.3:p.Val1313Ala