Canonical Allele Identifier: CA366242803

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522508G>T (hg19) ; chr6:g.157201374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201374G>T , CM000668.2:g.157201374G>T	GRCh38
NC_000006.11:g.157522508G>T , CM000668.1:g.157522508G>T	GRCh37
NC_000006.10:g.157564200G>T	NCBI36
NG_032093.1:g.428445G>T
NG_032093.2:g.428445G>T
NG_066624.1:g.430349G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4990G>T	ENSP00000055163.8:p.Gly1664Trp
ENST00000414678.8:c.5059G>T	ENSP00000412835.3:p.Gly1687Trp
ENST00000637015.2:c.5278G>T	ENSP00000489729.2:p.Gly1760Trp
ENST00000346085.10:c.5029G>T	ENSP00000344546.5:p.Gly1677Trp
ENST00000350026.10:c.4741G>T	ENSP00000055163.7:p.Gly1581Trp
ENST00000414678.7:c.3307G>T	ENSP00000412835.2:p.Gly1103Trp
ENST00000635849.1:c.2470G>T	ENSP00000490948.1:p.Gly824Trp
ENST00000635957.1:c.2101G>T	ENSP00000490385.1:p.Gly701Trp
ENST00000636227.1:n.3612G>T
ENST00000636254.1:n.1069G>T
ENST00000636930.2:c.5149G>T MANE Select	ENSP00000490491.2:p.Gly1717Trp
ENST00000636940.1:n.3146G>T
ENST00000637015.1:c.2517G>T
ENST00000637568.1:c.2431G>T
ENST00000637741.1:n.1815G>T
ENST00000637810.1:c.2491G>T	ENSP00000489636.1:p.Gly831Trp
ENST00000637904.1:c.2650G>T	ENSP00000490550.1:p.Gly884Trp
ENST00000647938.1:c.4780G>T	ENSP00000498155.1:p.Gly1594Trp
ENST00000346085.9:c.4780G>T	ENSP00000344546.4:p.Gly1594Trp
ENST00000350026.9:c.4741G>T	ENSP00000055163.7:p.Gly1581Trp
ENST00000414678.6:c.3307G>T	ENSP00000412835.2:p.Gly1103Trp
NM_017519.2:c.4741G>T	NP_059989.2:p.Gly1581Trp
NM_020732.3:c.4780G>T	NP_065783.3:p.Gly1594Trp
XM_005267069.3:c.4900G>T	XP_005267126.2:p.Gly1634Trp
XM_011535984.1:c.3979G>T	XP_011534286.1:p.Gly1327Trp
XM_011535985.1:c.3799G>T	XP_011534287.1:p.Gly1267Trp
XM_011535986.1:c.3559G>T	XP_011534288.1:p.Gly1187Trp
XM_011535987.1:c.3178G>T	XP_011534289.1:p.Gly1060Trp
XM_011535988.1:c.2041G>T	XP_011534290.1:p.Gly681Trp
NM_001346813.1:c.4900G>T	NP_001333742.1:p.Gly1634Trp
NM_001363725.1:c.2650G>T	NP_001350654.1:p.Gly884Trp
XM_011535984.2:c.5110G>T	XP_011534286.2:p.Gly1704Trp
XM_011535988.3:c.2041G>T	XP_011534290.1:p.Gly681Trp
XM_017011103.2:c.5011G>T	XP_016866592.1:p.Gly1671Trp
XM_017011104.1:c.4981G>T	XP_016866593.1:p.Gly1661Trp
XM_017011105.2:c.4951G>T	XP_016866594.1:p.Gly1651Trp
XM_017011106.2:c.4822G>T	XP_016866595.1:p.Gly1608Trp
XM_017011107.2:c.4801G>T	XP_016866596.1:p.Gly1601Trp
XR_002956289.1:n.5096G>T
NM_001363725.2:c.2650G>T	NP_001350654.1:p.Gly884Trp
NM_001371656.1:c.5029G>T	NP_001358585.1:p.Gly1677Trp
NM_001374820.1:c.5029G>T	NP_001361749.1:p.Gly1677Trp
NM_001374828.1:c.5149G>T MANE Select	NP_001361757.1:p.Gly1717Trp
NM_017519.3:c.4990G>T	NP_059989.3:p.Gly1664Trp