Canonical Allele Identifier: CA452978377

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522483C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201349C>G , CM000668.2:g.157201349C>G	GRCh38
NC_000006.11:g.157522483C>G , CM000668.1:g.157522483C>G	GRCh37
NC_000006.10:g.157564175C>G	NCBI36
NG_032093.1:g.428420C>G
NG_032093.2:g.428420C>G
NG_066624.1:g.430324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4965C>G	ENSP00000055163.8:p.Pro1655=
ENST00000414678.8:c.5034C>G	ENSP00000412835.3:p.Pro1678=
ENST00000637015.2:c.5253C>G	ENSP00000489729.2:p.Pro1751=
ENST00000346085.10:c.5004C>G	ENSP00000344546.5:p.Pro1668=
ENST00000350026.10:c.4716C>G	ENSP00000055163.7:p.Pro1572=
ENST00000414678.7:c.3282C>G	ENSP00000412835.2:p.Pro1094=
ENST00000635849.1:c.2445C>G	ENSP00000490948.1:p.Pro815=
ENST00000635957.1:c.2076C>G	ENSP00000490385.1:p.Pro692=
ENST00000636227.1:n.3587C>G
ENST00000636254.1:n.1044C>G
ENST00000636930.2:c.5124C>G MANE Select	ENSP00000490491.2:p.Pro1708=
ENST00000636940.1:n.3121C>G
ENST00000637015.1:c.2492C>G
ENST00000637568.1:c.2406C>G
ENST00000637741.1:n.1790C>G
ENST00000637810.1:c.2466C>G	ENSP00000489636.1:p.Pro822=
ENST00000637904.1:c.2625C>G	ENSP00000490550.1:p.Pro875=
ENST00000647938.1:c.4755C>G	ENSP00000498155.1:p.Pro1585=
ENST00000346085.9:c.4755C>G	ENSP00000344546.4:p.Pro1585=
ENST00000350026.9:c.4716C>G	ENSP00000055163.7:p.Pro1572=
ENST00000414678.6:c.3282C>G	ENSP00000412835.2:p.Pro1094=
NM_017519.2:c.4716C>G	NP_059989.2:p.Pro1572=
NM_020732.3:c.4755C>G	NP_065783.3:p.Pro1585=
XM_005267069.3:c.4875C>G	XP_005267126.2:p.Pro1625=
XM_011535984.1:c.3954C>G	XP_011534286.1:p.Pro1318=
XM_011535985.1:c.3774C>G	XP_011534287.1:p.Pro1258=
XM_011535986.1:c.3534C>G	XP_011534288.1:p.Pro1178=
XM_011535987.1:c.3153C>G	XP_011534289.1:p.Pro1051=
XM_011535988.1:c.2016C>G	XP_011534290.1:p.Pro672=
NM_001346813.1:c.4875C>G	NP_001333742.1:p.Pro1625=
NM_001363725.1:c.2625C>G	NP_001350654.1:p.Pro875=
XM_011535984.2:c.5085C>G	XP_011534286.2:p.Pro1695=
XM_011535988.3:c.2016C>G	XP_011534290.1:p.Pro672=
XM_017011103.2:c.4986C>G	XP_016866592.1:p.Pro1662=
XM_017011104.1:c.4956C>G	XP_016866593.1:p.Pro1652=
XM_017011105.2:c.4926C>G	XP_016866594.1:p.Pro1642=
XM_017011106.2:c.4797C>G	XP_016866595.1:p.Pro1599=
XM_017011107.2:c.4776C>G	XP_016866596.1:p.Pro1592=
XR_002956289.1:n.5071C>G
NM_001363725.2:c.2625C>G	NP_001350654.1:p.Pro875=
NM_001371656.1:c.5004C>G	NP_001358585.1:p.Pro1668=
NM_001374820.1:c.5004C>G	NP_001361749.1:p.Pro1668=
NM_001374828.1:c.5124C>G MANE Select	NP_001361757.1:p.Pro1708=
NM_017519.3:c.4965C>G	NP_059989.3:p.Pro1655=