Canonical Allele Identifier: CA366241242

Gene: ARID1B

Linked Data

• dbSNP Id: rs770643408
• MyVariant Identifiers: chr6:g.157522059C>G (hg19) ; chr6:g.157200925C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200925C>G , CM000668.2:g.157200925C>G	GRCh38
NC_000006.11:g.157522059C>G , CM000668.1:g.157522059C>G	GRCh37
NC_000006.10:g.157563751C>G	NCBI36
NG_032093.1:g.427996C>G
NG_032093.2:g.427996C>G
NG_066624.1:g.429900C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4541C>G	ENSP00000055163.8:p.Pro1514Arg
ENST00000414678.8:c.4610C>G	ENSP00000412835.3:p.Pro1537Arg
ENST00000637015.2:c.4829C>G	ENSP00000489729.2:p.Pro1610Arg
ENST00000346085.10:c.4580C>G	ENSP00000344546.5:p.Pro1527Arg
ENST00000350026.10:c.4292C>G	ENSP00000055163.7:p.Pro1431Arg
ENST00000414678.7:c.2858C>G	ENSP00000412835.2:p.Pro953Arg
ENST00000635849.1:c.2021C>G	ENSP00000490948.1:p.Pro674Arg
ENST00000635957.1:c.1652C>G	ENSP00000490385.1:p.Pro551Arg
ENST00000636227.1:n.3163C>G
ENST00000636254.1:n.620C>G
ENST00000636930.2:c.4700C>G MANE Select	ENSP00000490491.2:p.Pro1567Arg
ENST00000636940.1:n.2697C>G
ENST00000637015.1:c.2068C>G
ENST00000637568.1:c.1982C>G
ENST00000637741.1:n.1366C>G
ENST00000637810.1:c.2042C>G	ENSP00000489636.1:p.Pro681Arg
ENST00000637904.1:c.2201C>G	ENSP00000490550.1:p.Pro734Arg
ENST00000647938.1:c.4331C>G	ENSP00000498155.1:p.Pro1444Arg
ENST00000346085.9:c.4331C>G	ENSP00000344546.4:p.Pro1444Arg
ENST00000350026.9:c.4292C>G	ENSP00000055163.7:p.Pro1431Arg
ENST00000414678.6:c.2858C>G	ENSP00000412835.2:p.Pro953Arg
NM_017519.2:c.4292C>G	NP_059989.2:p.Pro1431Arg
NM_020732.3:c.4331C>G	NP_065783.3:p.Pro1444Arg
XM_005267069.3:c.4451C>G	XP_005267126.2:p.Pro1484Arg
XM_011535984.1:c.3530C>G	XP_011534286.1:p.Pro1177Arg
XM_011535985.1:c.3350C>G	XP_011534287.1:p.Pro1117Arg
XM_011535986.1:c.3110C>G	XP_011534288.1:p.Pro1037Arg
XM_011535987.1:c.2729C>G	XP_011534289.1:p.Pro910Arg
XM_011535988.1:c.1592C>G	XP_011534290.1:p.Pro531Arg
NM_001346813.1:c.4451C>G	NP_001333742.1:p.Pro1484Arg
NM_001363725.1:c.2201C>G	NP_001350654.1:p.Pro734Arg
XM_011535984.2:c.4661C>G	XP_011534286.2:p.Pro1554Arg
XM_011535988.3:c.1592C>G	XP_011534290.1:p.Pro531Arg
XM_017011103.2:c.4562C>G	XP_016866592.1:p.Pro1521Arg
XM_017011104.1:c.4532C>G	XP_016866593.1:p.Pro1511Arg
XM_017011105.2:c.4502C>G	XP_016866594.1:p.Pro1501Arg
XM_017011106.2:c.4373C>G	XP_016866595.1:p.Pro1458Arg
XM_017011107.2:c.4352C>G	XP_016866596.1:p.Pro1451Arg
XR_002956289.1:n.4647C>G
NM_001363725.2:c.2201C>G	NP_001350654.1:p.Pro734Arg
NM_001371656.1:c.4580C>G	NP_001358585.1:p.Pro1527Arg
NM_001374820.1:c.4580C>G	NP_001361749.1:p.Pro1527Arg
NM_001374828.1:c.4700C>G MANE Select	NP_001361757.1:p.Pro1567Arg
NM_017519.3:c.4541C>G	NP_059989.3:p.Pro1514Arg