Canonical Allele Identifier: CA366234099

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510827A>C (hg19) ; chr6:g.157189693A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189693A>C , CM000668.2:g.157189693A>C	GRCh38
NC_000006.11:g.157510827A>C , CM000668.1:g.157510827A>C	GRCh37
NC_000006.10:g.157552519A>C	NCBI36
NG_032093.1:g.416764A>C
NG_032093.2:g.416764A>C
NG_066624.1:g.418668A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3812A>C	ENSP00000055163.8:p.Asn1271Thr
ENST00000414678.8:c.3881A>C	ENSP00000412835.3:p.Asn1294Thr
ENST00000637015.2:c.4100A>C	ENSP00000489729.2:p.Asn1367Thr
ENST00000346085.10:c.3851A>C	ENSP00000344546.5:p.Asn1284Thr
ENST00000350026.10:c.3563A>C	ENSP00000055163.7:p.Asn1188Thr
ENST00000414678.7:c.2129A>C	ENSP00000412835.2:p.Asn710Thr
ENST00000635849.1:c.1292A>C	ENSP00000490948.1:p.Asn431Thr
ENST00000635957.1:c.926A>C	ENSP00000490385.1:p.Asn309Thr
ENST00000636930.2:c.3971A>C MANE Select	ENSP00000490491.2:p.Asn1324Thr
ENST00000636940.1:n.1968A>C
ENST00000637015.1:c.1339A>C
ENST00000637568.1:c.1253A>C
ENST00000637741.1:n.637A>C
ENST00000637810.1:c.1313A>C	ENSP00000489636.1:p.Asn438Thr
ENST00000637904.1:c.1472A>C	ENSP00000490550.1:p.Asn491Thr
ENST00000647938.1:c.3602A>C	ENSP00000498155.1:p.Asn1201Thr
ENST00000346085.9:c.3602A>C	ENSP00000344546.4:p.Asn1201Thr
ENST00000350026.9:c.3563A>C	ENSP00000055163.7:p.Asn1188Thr
ENST00000414678.6:c.2129A>C	ENSP00000412835.2:p.Asn710Thr
NM_017519.2:c.3563A>C	NP_059989.2:p.Asn1188Thr
NM_020732.3:c.3602A>C	NP_065783.3:p.Asn1201Thr
XM_005267069.3:c.3722A>C	XP_005267126.2:p.Asn1241Thr
XM_011535984.1:c.2801A>C	XP_011534286.1:p.Asn934Thr
XM_011535985.1:c.2621A>C	XP_011534287.1:p.Asn874Thr
XM_011535986.1:c.2381A>C	XP_011534288.1:p.Asn794Thr
XM_011535987.1:c.2000A>C	XP_011534289.1:p.Asn667Thr
XM_011535988.1:c.863A>C	XP_011534290.1:p.Asn288Thr
NM_001346813.1:c.3722A>C	NP_001333742.1:p.Asn1241Thr
NM_001363725.1:c.1472A>C	NP_001350654.1:p.Asn491Thr
XM_011535984.2:c.3932A>C	XP_011534286.2:p.Asn1311Thr
XM_011535988.3:c.863A>C	XP_011534290.1:p.Asn288Thr
XM_017011103.2:c.3833A>C	XP_016866592.1:p.Asn1278Thr
XM_017011104.1:c.3803A>C	XP_016866593.1:p.Asn1268Thr
XM_017011105.2:c.3773A>C	XP_016866594.1:p.Asn1258Thr
XM_017011106.2:c.3644A>C	XP_016866595.1:p.Asn1215Thr
XM_017011107.2:c.3623A>C	XP_016866596.1:p.Asn1208Thr
XR_002956289.1:n.4015A>C
NM_001363725.2:c.1472A>C	NP_001350654.1:p.Asn491Thr
NM_001371656.1:c.3851A>C	NP_001358585.1:p.Asn1284Thr
NM_001374820.1:c.3851A>C	NP_001361749.1:p.Asn1284Thr
NM_001374828.1:c.3971A>C MANE Select	NP_001361757.1:p.Asn1324Thr
NM_017519.3:c.3812A>C	NP_059989.3:p.Asn1271Thr