Canonical Allele Identifier: CA366242879

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522523C>T (hg19) ; chr6:g.157201389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201389C>T , CM000668.2:g.157201389C>T	GRCh38
NC_000006.11:g.157522523C>T , CM000668.1:g.157522523C>T	GRCh37
NC_000006.10:g.157564215C>T	NCBI36
NG_032093.1:g.428460C>T
NG_032093.2:g.428460C>T
NG_066624.1:g.430364C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5005C>T	ENSP00000055163.8:p.Pro1669Ser
ENST00000414678.8:c.5074C>T	ENSP00000412835.3:p.Pro1692Ser
ENST00000637015.2:c.5293C>T	ENSP00000489729.2:p.Pro1765Ser
ENST00000346085.10:c.5044C>T	ENSP00000344546.5:p.Pro1682Ser
ENST00000350026.10:c.4756C>T	ENSP00000055163.7:p.Pro1586Ser
ENST00000414678.7:c.3322C>T	ENSP00000412835.2:p.Pro1108Ser
ENST00000635849.1:c.2485C>T	ENSP00000490948.1:p.Pro829Ser
ENST00000635957.1:c.2116C>T	ENSP00000490385.1:p.Pro706Ser
ENST00000636227.1:n.3627C>T
ENST00000636254.1:n.1084C>T
ENST00000636930.2:c.5164C>T MANE Select	ENSP00000490491.2:p.Pro1722Ser
ENST00000636940.1:n.3161C>T
ENST00000637015.1:c.2532C>T
ENST00000637568.1:c.2446C>T
ENST00000637741.1:n.1830C>T
ENST00000637810.1:c.2506C>T	ENSP00000489636.1:p.Pro836Ser
ENST00000637904.1:c.2665C>T	ENSP00000490550.1:p.Pro889Ser
ENST00000647938.1:c.4795C>T	ENSP00000498155.1:p.Pro1599Ser
ENST00000346085.9:c.4795C>T	ENSP00000344546.4:p.Pro1599Ser
ENST00000350026.9:c.4756C>T	ENSP00000055163.7:p.Pro1586Ser
ENST00000414678.6:c.3322C>T	ENSP00000412835.2:p.Pro1108Ser
NM_017519.2:c.4756C>T	NP_059989.2:p.Pro1586Ser
NM_020732.3:c.4795C>T	NP_065783.3:p.Pro1599Ser
XM_005267069.3:c.4915C>T	XP_005267126.2:p.Pro1639Ser
XM_011535984.1:c.3994C>T	XP_011534286.1:p.Pro1332Ser
XM_011535985.1:c.3814C>T	XP_011534287.1:p.Pro1272Ser
XM_011535986.1:c.3574C>T	XP_011534288.1:p.Pro1192Ser
XM_011535987.1:c.3193C>T	XP_011534289.1:p.Pro1065Ser
XM_011535988.1:c.2056C>T	XP_011534290.1:p.Pro686Ser
NM_001346813.1:c.4915C>T	NP_001333742.1:p.Pro1639Ser
NM_001363725.1:c.2665C>T	NP_001350654.1:p.Pro889Ser
XM_011535984.2:c.5125C>T	XP_011534286.2:p.Pro1709Ser
XM_011535988.3:c.2056C>T	XP_011534290.1:p.Pro686Ser
XM_017011103.2:c.5026C>T	XP_016866592.1:p.Pro1676Ser
XM_017011104.1:c.4996C>T	XP_016866593.1:p.Pro1666Ser
XM_017011105.2:c.4966C>T	XP_016866594.1:p.Pro1656Ser
XM_017011106.2:c.4837C>T	XP_016866595.1:p.Pro1613Ser
XM_017011107.2:c.4816C>T	XP_016866596.1:p.Pro1606Ser
XR_002956289.1:n.5111C>T
NM_001363725.2:c.2665C>T	NP_001350654.1:p.Pro889Ser
NM_001371656.1:c.5044C>T	NP_001358585.1:p.Pro1682Ser
NM_001374820.1:c.5044C>T	NP_001361749.1:p.Pro1682Ser
NM_001374828.1:c.5164C>T MANE Select	NP_001361757.1:p.Pro1722Ser
NM_017519.3:c.5005C>T	NP_059989.3:p.Pro1669Ser