Canonical Allele Identifier: CA366242703

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376167
• MyVariant Identifiers: chr6:g.157522487G>C (hg19) ; chr6:g.157201353G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201353G>C , CM000668.2:g.157201353G>C	GRCh38
NC_000006.11:g.157522487G>C , CM000668.1:g.157522487G>C	GRCh37
NC_000006.10:g.157564179G>C	NCBI36
NG_032093.1:g.428424G>C
NG_032093.2:g.428424G>C
NG_066624.1:g.430328G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4969G>C	ENSP00000055163.8:p.Val1657Leu
ENST00000414678.8:c.5038G>C	ENSP00000412835.3:p.Val1680Leu
ENST00000637015.2:c.5257G>C	ENSP00000489729.2:p.Val1753Leu
ENST00000346085.10:c.5008G>C	ENSP00000344546.5:p.Val1670Leu
ENST00000350026.10:c.4720G>C	ENSP00000055163.7:p.Val1574Leu
ENST00000414678.7:c.3286G>C	ENSP00000412835.2:p.Val1096Leu
ENST00000635849.1:c.2449G>C	ENSP00000490948.1:p.Val817Leu
ENST00000635957.1:c.2080G>C	ENSP00000490385.1:p.Val694Leu
ENST00000636227.1:n.3591G>C
ENST00000636254.1:n.1048G>C
ENST00000636930.2:c.5128G>C MANE Select	ENSP00000490491.2:p.Val1710Leu
ENST00000636940.1:n.3125G>C
ENST00000637015.1:c.2496G>C
ENST00000637568.1:c.2410G>C
ENST00000637741.1:n.1794G>C
ENST00000637810.1:c.2470G>C	ENSP00000489636.1:p.Val824Leu
ENST00000637904.1:c.2629G>C	ENSP00000490550.1:p.Val877Leu
ENST00000647938.1:c.4759G>C	ENSP00000498155.1:p.Val1587Leu
ENST00000346085.9:c.4759G>C	ENSP00000344546.4:p.Val1587Leu
ENST00000350026.9:c.4720G>C	ENSP00000055163.7:p.Val1574Leu
ENST00000414678.6:c.3286G>C	ENSP00000412835.2:p.Val1096Leu
NM_017519.2:c.4720G>C	NP_059989.2:p.Val1574Leu
NM_020732.3:c.4759G>C	NP_065783.3:p.Val1587Leu
XM_005267069.3:c.4879G>C	XP_005267126.2:p.Val1627Leu
XM_011535984.1:c.3958G>C	XP_011534286.1:p.Val1320Leu
XM_011535985.1:c.3778G>C	XP_011534287.1:p.Val1260Leu
XM_011535986.1:c.3538G>C	XP_011534288.1:p.Val1180Leu
XM_011535987.1:c.3157G>C	XP_011534289.1:p.Val1053Leu
XM_011535988.1:c.2020G>C	XP_011534290.1:p.Val674Leu
NM_001346813.1:c.4879G>C	NP_001333742.1:p.Val1627Leu
NM_001363725.1:c.2629G>C	NP_001350654.1:p.Val877Leu
XM_011535984.2:c.5089G>C	XP_011534286.2:p.Val1697Leu
XM_011535988.3:c.2020G>C	XP_011534290.1:p.Val674Leu
XM_017011103.2:c.4990G>C	XP_016866592.1:p.Val1664Leu
XM_017011104.1:c.4960G>C	XP_016866593.1:p.Val1654Leu
XM_017011105.2:c.4930G>C	XP_016866594.1:p.Val1644Leu
XM_017011106.2:c.4801G>C	XP_016866595.1:p.Val1601Leu
XM_017011107.2:c.4780G>C	XP_016866596.1:p.Val1594Leu
XR_002956289.1:n.5075G>C
NM_001363725.2:c.2629G>C	NP_001350654.1:p.Val877Leu
NM_001371656.1:c.5008G>C	NP_001358585.1:p.Val1670Leu
NM_001374820.1:c.5008G>C	NP_001361749.1:p.Val1670Leu
NM_001374828.1:c.5128G>C MANE Select	NP_001361757.1:p.Val1710Leu
NM_017519.3:c.4969G>C	NP_059989.3:p.Val1657Leu