Canonical Allele Identifier: CA366241479

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522143C>T (hg19) ; chr6:g.157201009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201009C>T , CM000668.2:g.157201009C>T	GRCh38
NC_000006.11:g.157522143C>T , CM000668.1:g.157522143C>T	GRCh37
NC_000006.10:g.157563835C>T	NCBI36
NG_032093.1:g.428080C>T
NG_032093.2:g.428080C>T
NG_066624.1:g.429984C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4625C>T	ENSP00000055163.8:p.Pro1542Leu
ENST00000414678.8:c.4694C>T	ENSP00000412835.3:p.Pro1565Leu
ENST00000637015.2:c.4913C>T	ENSP00000489729.2:p.Pro1638Leu
ENST00000346085.10:c.4664C>T	ENSP00000344546.5:p.Pro1555Leu
ENST00000350026.10:c.4376C>T	ENSP00000055163.7:p.Pro1459Leu
ENST00000414678.7:c.2942C>T	ENSP00000412835.2:p.Pro981Leu
ENST00000635849.1:c.2105C>T	ENSP00000490948.1:p.Pro702Leu
ENST00000635957.1:c.1736C>T	ENSP00000490385.1:p.Pro579Leu
ENST00000636227.1:n.3247C>T
ENST00000636254.1:n.704C>T
ENST00000636930.2:c.4784C>T MANE Select	ENSP00000490491.2:p.Pro1595Leu
ENST00000636940.1:n.2781C>T
ENST00000637015.1:c.2152C>T
ENST00000637568.1:c.2066C>T
ENST00000637741.1:n.1450C>T
ENST00000637810.1:c.2126C>T	ENSP00000489636.1:p.Pro709Leu
ENST00000637904.1:c.2285C>T	ENSP00000490550.1:p.Pro762Leu
ENST00000647938.1:c.4415C>T	ENSP00000498155.1:p.Pro1472Leu
ENST00000346085.9:c.4415C>T	ENSP00000344546.4:p.Pro1472Leu
ENST00000350026.9:c.4376C>T	ENSP00000055163.7:p.Pro1459Leu
ENST00000414678.6:c.2942C>T	ENSP00000412835.2:p.Pro981Leu
NM_017519.2:c.4376C>T	NP_059989.2:p.Pro1459Leu
NM_020732.3:c.4415C>T	NP_065783.3:p.Pro1472Leu
XM_005267069.3:c.4535C>T	XP_005267126.2:p.Pro1512Leu
XM_011535984.1:c.3614C>T	XP_011534286.1:p.Pro1205Leu
XM_011535985.1:c.3434C>T	XP_011534287.1:p.Pro1145Leu
XM_011535986.1:c.3194C>T	XP_011534288.1:p.Pro1065Leu
XM_011535987.1:c.2813C>T	XP_011534289.1:p.Pro938Leu
XM_011535988.1:c.1676C>T	XP_011534290.1:p.Pro559Leu
NM_001346813.1:c.4535C>T	NP_001333742.1:p.Pro1512Leu
NM_001363725.1:c.2285C>T	NP_001350654.1:p.Pro762Leu
XM_011535984.2:c.4745C>T	XP_011534286.2:p.Pro1582Leu
XM_011535988.3:c.1676C>T	XP_011534290.1:p.Pro559Leu
XM_017011103.2:c.4646C>T	XP_016866592.1:p.Pro1549Leu
XM_017011104.1:c.4616C>T	XP_016866593.1:p.Pro1539Leu
XM_017011105.2:c.4586C>T	XP_016866594.1:p.Pro1529Leu
XM_017011106.2:c.4457C>T	XP_016866595.1:p.Pro1486Leu
XM_017011107.2:c.4436C>T	XP_016866596.1:p.Pro1479Leu
XR_002956289.1:n.4731C>T
NM_001363725.2:c.2285C>T	NP_001350654.1:p.Pro762Leu
NM_001371656.1:c.4664C>T	NP_001358585.1:p.Pro1555Leu
NM_001374820.1:c.4664C>T	NP_001361749.1:p.Pro1555Leu
NM_001374828.1:c.4784C>T MANE Select	NP_001361757.1:p.Pro1595Leu
NM_017519.3:c.4625C>T	NP_059989.3:p.Pro1542Leu