Canonical Allele Identifier: CA366241979

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522232C>A (hg19) ; chr6:g.157201098C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201098C>A , CM000668.2:g.157201098C>A	GRCh38
NC_000006.11:g.157522232C>A , CM000668.1:g.157522232C>A	GRCh37
NC_000006.10:g.157563924C>A	NCBI36
NG_032093.1:g.428169C>A
NG_032093.2:g.428169C>A
NG_066624.1:g.430073C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4714C>A	ENSP00000055163.8:p.Pro1572Thr
ENST00000414678.8:c.4783C>A	ENSP00000412835.3:p.Pro1595Thr
ENST00000637015.2:c.5002C>A	ENSP00000489729.2:p.Pro1668Thr
ENST00000346085.10:c.4753C>A	ENSP00000344546.5:p.Pro1585Thr
ENST00000350026.10:c.4465C>A	ENSP00000055163.7:p.Pro1489Thr
ENST00000414678.7:c.3031C>A	ENSP00000412835.2:p.Pro1011Thr
ENST00000635849.1:c.2194C>A	ENSP00000490948.1:p.Pro732Thr
ENST00000635957.1:c.1825C>A	ENSP00000490385.1:p.Pro609Thr
ENST00000636227.1:n.3336C>A
ENST00000636254.1:n.793C>A
ENST00000636930.2:c.4873C>A MANE Select	ENSP00000490491.2:p.Pro1625Thr
ENST00000636940.1:n.2870C>A
ENST00000637015.1:c.2241C>A
ENST00000637568.1:c.2155C>A
ENST00000637741.1:n.1539C>A
ENST00000637810.1:c.2215C>A	ENSP00000489636.1:p.Pro739Thr
ENST00000637904.1:c.2374C>A	ENSP00000490550.1:p.Pro792Thr
ENST00000647938.1:c.4504C>A	ENSP00000498155.1:p.Pro1502Thr
ENST00000346085.9:c.4504C>A	ENSP00000344546.4:p.Pro1502Thr
ENST00000350026.9:c.4465C>A	ENSP00000055163.7:p.Pro1489Thr
ENST00000414678.6:c.3031C>A	ENSP00000412835.2:p.Pro1011Thr
NM_017519.2:c.4465C>A	NP_059989.2:p.Pro1489Thr
NM_020732.3:c.4504C>A	NP_065783.3:p.Pro1502Thr
XM_005267069.3:c.4624C>A	XP_005267126.2:p.Pro1542Thr
XM_011535984.1:c.3703C>A	XP_011534286.1:p.Pro1235Thr
XM_011535985.1:c.3523C>A	XP_011534287.1:p.Pro1175Thr
XM_011535986.1:c.3283C>A	XP_011534288.1:p.Pro1095Thr
XM_011535987.1:c.2902C>A	XP_011534289.1:p.Pro968Thr
XM_011535988.1:c.1765C>A	XP_011534290.1:p.Pro589Thr
NM_001346813.1:c.4624C>A	NP_001333742.1:p.Pro1542Thr
NM_001363725.1:c.2374C>A	NP_001350654.1:p.Pro792Thr
XM_011535984.2:c.4834C>A	XP_011534286.2:p.Pro1612Thr
XM_011535988.3:c.1765C>A	XP_011534290.1:p.Pro589Thr
XM_017011103.2:c.4735C>A	XP_016866592.1:p.Pro1579Thr
XM_017011104.1:c.4705C>A	XP_016866593.1:p.Pro1569Thr
XM_017011105.2:c.4675C>A	XP_016866594.1:p.Pro1559Thr
XM_017011106.2:c.4546C>A	XP_016866595.1:p.Pro1516Thr
XM_017011107.2:c.4525C>A	XP_016866596.1:p.Pro1509Thr
XR_002956289.1:n.4820C>A
NM_001363725.2:c.2374C>A	NP_001350654.1:p.Pro792Thr
NM_001371656.1:c.4753C>A	NP_001358585.1:p.Pro1585Thr
NM_001374820.1:c.4753C>A	NP_001361749.1:p.Pro1585Thr
NM_001374828.1:c.4873C>A MANE Select	NP_001361757.1:p.Pro1625Thr
NM_017519.3:c.4714C>A	NP_059989.3:p.Pro1572Thr