Canonical Allele Identifier: CA366242874

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794110328
• gnomAD v4: 6-157201389-C-A
• MyVariant Identifiers: chr6:g.157522523C>A (hg19) ; chr6:g.157201389C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5005C>A	ENSP00000055163.8:p.Pro1669Thr
ENST00000414678.8:c.5074C>A	ENSP00000412835.3:p.Pro1692Thr
ENST00000637015.2:c.5293C>A	ENSP00000489729.2:p.Pro1765Thr
ENST00000346085.10:c.5044C>A	ENSP00000344546.5:p.Pro1682Thr
ENST00000350026.10:c.4756C>A	ENSP00000055163.7:p.Pro1586Thr
ENST00000414678.7:c.3322C>A	ENSP00000412835.2:p.Pro1108Thr
ENST00000635849.1:c.2485C>A	ENSP00000490948.1:p.Pro829Thr
ENST00000635957.1:c.2116C>A	ENSP00000490385.1:p.Pro706Thr
ENST00000636227.1:n.3627C>A
ENST00000636254.1:n.1084C>A
ENST00000636930.2:c.5164C>A MANE Select	ENSP00000490491.2:p.Pro1722Thr
ENST00000636940.1:n.3161C>A
ENST00000637015.1:c.2532C>A
ENST00000637568.1:c.2446C>A
ENST00000637741.1:n.1830C>A
ENST00000637810.1:c.2506C>A	ENSP00000489636.1:p.Pro836Thr
ENST00000637904.1:c.2665C>A	ENSP00000490550.1:p.Pro889Thr
ENST00000647938.1:c.4795C>A	ENSP00000498155.1:p.Pro1599Thr
ENST00000346085.9:c.4795C>A	ENSP00000344546.4:p.Pro1599Thr
ENST00000350026.9:c.4756C>A	ENSP00000055163.7:p.Pro1586Thr
ENST00000414678.6:c.3322C>A	ENSP00000412835.2:p.Pro1108Thr
NM_017519.2:c.4756C>A	NP_059989.2:p.Pro1586Thr
NM_020732.3:c.4795C>A	NP_065783.3:p.Pro1599Thr
XM_005267069.3:c.4915C>A	XP_005267126.2:p.Pro1639Thr
XM_011535984.1:c.3994C>A	XP_011534286.1:p.Pro1332Thr
XM_011535985.1:c.3814C>A	XP_011534287.1:p.Pro1272Thr
XM_011535986.1:c.3574C>A	XP_011534288.1:p.Pro1192Thr
XM_011535987.1:c.3193C>A	XP_011534289.1:p.Pro1065Thr
XM_011535988.1:c.2056C>A	XP_011534290.1:p.Pro686Thr
NM_001346813.1:c.4915C>A	NP_001333742.1:p.Pro1639Thr
NM_001363725.1:c.2665C>A	NP_001350654.1:p.Pro889Thr
XM_011535984.2:c.5125C>A	XP_011534286.2:p.Pro1709Thr
XM_011535988.3:c.2056C>A	XP_011534290.1:p.Pro686Thr
XM_017011103.2:c.5026C>A	XP_016866592.1:p.Pro1676Thr
XM_017011104.1:c.4996C>A	XP_016866593.1:p.Pro1666Thr
XM_017011105.2:c.4966C>A	XP_016866594.1:p.Pro1656Thr
XM_017011106.2:c.4837C>A	XP_016866595.1:p.Pro1613Thr
XM_017011107.2:c.4816C>A	XP_016866596.1:p.Pro1606Thr
XR_002956289.1:n.5111C>A
NM_001363725.2:c.2665C>A	NP_001350654.1:p.Pro889Thr
NM_001371656.1:c.5044C>A	NP_001358585.1:p.Pro1682Thr
NM_001374820.1:c.5044C>A	NP_001361749.1:p.Pro1682Thr
NM_001374828.1:c.5164C>A MANE Select	NP_001361757.1:p.Pro1722Thr
NM_017519.3:c.5005C>A	NP_059989.3:p.Pro1669Thr