Canonical Allele Identifier: CA366242963

Gene: ARID1B

Linked Data

• dbSNP Id: rs1206706709
• MyVariant Identifiers: chr6:g.157522539G>C (hg19) ; chr6:g.157201405G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201405G>C , CM000668.2:g.157201405G>C	GRCh38
NC_000006.11:g.157522539G>C , CM000668.1:g.157522539G>C	GRCh37
NC_000006.10:g.157564231G>C	NCBI36
NG_032093.1:g.428476G>C
NG_032093.2:g.428476G>C
NG_066624.1:g.430380G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5021G>C	ENSP00000055163.8:p.Arg1674Thr
ENST00000414678.8:c.5090G>C	ENSP00000412835.3:p.Arg1697Thr
ENST00000637015.2:c.5309G>C	ENSP00000489729.2:p.Arg1770Thr
ENST00000346085.10:c.5060G>C	ENSP00000344546.5:p.Arg1687Thr
ENST00000350026.10:c.4772G>C	ENSP00000055163.7:p.Arg1591Thr
ENST00000414678.7:c.3338G>C	ENSP00000412835.2:p.Arg1113Thr
ENST00000635849.1:c.2501G>C	ENSP00000490948.1:p.Arg834Thr
ENST00000635957.1:c.2132G>C	ENSP00000490385.1:p.Arg711Thr
ENST00000636227.1:n.3643G>C
ENST00000636254.1:n.1100G>C
ENST00000636930.2:c.5180G>C MANE Select	ENSP00000490491.2:p.Arg1727Thr
ENST00000636940.1:n.3177G>C
ENST00000637015.1:c.2548G>C
ENST00000637568.1:c.2462G>C
ENST00000637741.1:n.1846G>C
ENST00000637810.1:c.2522G>C	ENSP00000489636.1:p.Arg841Thr
ENST00000637904.1:c.2681G>C	ENSP00000490550.1:p.Arg894Thr
ENST00000647938.1:c.4811G>C	ENSP00000498155.1:p.Arg1604Thr
ENST00000346085.9:c.4811G>C	ENSP00000344546.4:p.Arg1604Thr
ENST00000350026.9:c.4772G>C	ENSP00000055163.7:p.Arg1591Thr
ENST00000414678.6:c.3338G>C	ENSP00000412835.2:p.Arg1113Thr
NM_017519.2:c.4772G>C	NP_059989.2:p.Arg1591Thr
NM_020732.3:c.4811G>C	NP_065783.3:p.Arg1604Thr
XM_005267069.3:c.4931G>C	XP_005267126.2:p.Arg1644Thr
XM_011535984.1:c.4010G>C	XP_011534286.1:p.Arg1337Thr
XM_011535985.1:c.3830G>C	XP_011534287.1:p.Arg1277Thr
XM_011535986.1:c.3590G>C	XP_011534288.1:p.Arg1197Thr
XM_011535987.1:c.3209G>C	XP_011534289.1:p.Arg1070Thr
XM_011535988.1:c.2072G>C	XP_011534290.1:p.Arg691Thr
NM_001346813.1:c.4931G>C	NP_001333742.1:p.Arg1644Thr
NM_001363725.1:c.2681G>C	NP_001350654.1:p.Arg894Thr
XM_011535984.2:c.5141G>C	XP_011534286.2:p.Arg1714Thr
XM_011535988.3:c.2072G>C	XP_011534290.1:p.Arg691Thr
XM_017011103.2:c.5042G>C	XP_016866592.1:p.Arg1681Thr
XM_017011104.1:c.5012G>C	XP_016866593.1:p.Arg1671Thr
XM_017011105.2:c.4982G>C	XP_016866594.1:p.Arg1661Thr
XM_017011106.2:c.4853G>C	XP_016866595.1:p.Arg1618Thr
XM_017011107.2:c.4832G>C	XP_016866596.1:p.Arg1611Thr
XR_002956289.1:n.5127G>C
NM_001363725.2:c.2681G>C	NP_001350654.1:p.Arg894Thr
NM_001371656.1:c.5060G>C	NP_001358585.1:p.Arg1687Thr
NM_001374820.1:c.5060G>C	NP_001361749.1:p.Arg1687Thr
NM_001374828.1:c.5180G>C MANE Select	NP_001361757.1:p.Arg1727Thr
NM_017519.3:c.5021G>C	NP_059989.3:p.Arg1674Thr