Canonical Allele Identifier: CA452978321

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375844
• MyVariant Identifiers: chr6:g.157522447T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201313T>C , CM000668.2:g.157201313T>C	GRCh38
NC_000006.11:g.157522447T>C , CM000668.1:g.157522447T>C	GRCh37
NC_000006.10:g.157564139T>C	NCBI36
NG_032093.1:g.428384T>C
NG_032093.2:g.428384T>C
NG_066624.1:g.430288T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4929T>C	ENSP00000055163.8:p.Pro1643=
ENST00000414678.8:c.4998T>C	ENSP00000412835.3:p.Pro1666=
ENST00000637015.2:c.5217T>C	ENSP00000489729.2:p.Pro1739=
ENST00000346085.10:c.4968T>C	ENSP00000344546.5:p.Pro1656=
ENST00000350026.10:c.4680T>C	ENSP00000055163.7:p.Pro1560=
ENST00000414678.7:c.3246T>C	ENSP00000412835.2:p.Pro1082=
ENST00000635849.1:c.2409T>C	ENSP00000490948.1:p.Pro803=
ENST00000635957.1:c.2040T>C	ENSP00000490385.1:p.Pro680=
ENST00000636227.1:n.3551T>C
ENST00000636254.1:n.1008T>C
ENST00000636930.2:c.5088T>C MANE Select	ENSP00000490491.2:p.Pro1696=
ENST00000636940.1:n.3085T>C
ENST00000637015.1:c.2456T>C
ENST00000637568.1:c.2370T>C
ENST00000637741.1:n.1754T>C
ENST00000637810.1:c.2430T>C	ENSP00000489636.1:p.Pro810=
ENST00000637904.1:c.2589T>C	ENSP00000490550.1:p.Pro863=
ENST00000647938.1:c.4719T>C	ENSP00000498155.1:p.Pro1573=
ENST00000346085.9:c.4719T>C	ENSP00000344546.4:p.Pro1573=
ENST00000350026.9:c.4680T>C	ENSP00000055163.7:p.Pro1560=
ENST00000414678.6:c.3246T>C	ENSP00000412835.2:p.Pro1082=
NM_017519.2:c.4680T>C	NP_059989.2:p.Pro1560=
NM_020732.3:c.4719T>C	NP_065783.3:p.Pro1573=
XM_005267069.3:c.4839T>C	XP_005267126.2:p.Pro1613=
XM_011535984.1:c.3918T>C	XP_011534286.1:p.Pro1306=
XM_011535985.1:c.3738T>C	XP_011534287.1:p.Pro1246=
XM_011535986.1:c.3498T>C	XP_011534288.1:p.Pro1166=
XM_011535987.1:c.3117T>C	XP_011534289.1:p.Pro1039=
XM_011535988.1:c.1980T>C	XP_011534290.1:p.Pro660=
NM_001346813.1:c.4839T>C	NP_001333742.1:p.Pro1613=
NM_001363725.1:c.2589T>C	NP_001350654.1:p.Pro863=
XM_011535984.2:c.5049T>C	XP_011534286.2:p.Pro1683=
XM_011535988.3:c.1980T>C	XP_011534290.1:p.Pro660=
XM_017011103.2:c.4950T>C	XP_016866592.1:p.Pro1650=
XM_017011104.1:c.4920T>C	XP_016866593.1:p.Pro1640=
XM_017011105.2:c.4890T>C	XP_016866594.1:p.Pro1630=
XM_017011106.2:c.4761T>C	XP_016866595.1:p.Pro1587=
XM_017011107.2:c.4740T>C	XP_016866596.1:p.Pro1580=
XR_002956289.1:n.5035T>C
NM_001363725.2:c.2589T>C	NP_001350654.1:p.Pro863=
NM_001371656.1:c.4968T>C	NP_001358585.1:p.Pro1656=
NM_001374820.1:c.4968T>C	NP_001361749.1:p.Pro1656=
NM_001374828.1:c.5088T>C MANE Select	NP_001361757.1:p.Pro1696=
NM_017519.3:c.4929T>C	NP_059989.3:p.Pro1643=