Canonical Allele Identifier: CA366227503

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502176A>T (hg19) ; chr6:g.157181042A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181042A>T , CM000668.2:g.157181042A>T	GRCh38
NC_000006.11:g.157502176A>T , CM000668.1:g.157502176A>T	GRCh37
NC_000006.10:g.157543868A>T	NCBI36
NG_032093.1:g.408113A>T
NG_032093.2:g.408113A>T
NG_066624.1:g.410017A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3419A>T	ENSP00000055163.8:p.Lys1140Met
ENST00000414678.8:c.3488A>T	ENSP00000412835.3:p.Lys1163Met
ENST00000637015.2:c.3707A>T	ENSP00000489729.2:p.Lys1236Met
ENST00000319584.11:c.1592A>T	ENSP00000313006.7:p.Lys531Met
ENST00000346085.10:c.3458A>T	ENSP00000344546.5:p.Lys1153Met
ENST00000350026.10:c.3170A>T	ENSP00000055163.7:p.Lys1057Met
ENST00000414678.7:c.1736A>T	ENSP00000412835.2:p.Lys579Met
ENST00000635849.1:c.899A>T	ENSP00000490948.1:p.Lys300Met
ENST00000635957.1:c.533A>T	ENSP00000490385.1:p.Lys178Met
ENST00000636930.2:c.3578A>T MANE Select	ENSP00000490491.2:p.Lys1193Met
ENST00000636940.1:n.1575A>T
ENST00000637015.1:c.946A>T
ENST00000637568.1:c.860A>T
ENST00000637741.1:n.244A>T
ENST00000637810.1:c.920A>T	ENSP00000489636.1:p.Lys307Met
ENST00000637904.1:c.1079A>T	ENSP00000490550.1:p.Lys360Met
ENST00000647938.1:c.3209A>T	ENSP00000498155.1:p.Lys1070Met
ENST00000319584.10:c.1595A>T	ENSP00000313006.6:p.Lys532Met
ENST00000346085.9:c.3209A>T	ENSP00000344546.4:p.Lys1070Met
ENST00000350026.9:c.3170A>T	ENSP00000055163.7:p.Lys1057Met
ENST00000400790.3:c.371A>T	ENSP00000383596.3:p.Lys124Met
ENST00000414678.6:c.1736A>T	ENSP00000412835.2:p.Lys579Met
ENST00000478761.3:c.780A>T
NM_017519.2:c.3170A>T	NP_059989.2:p.Lys1057Met
NM_020732.3:c.3209A>T	NP_065783.3:p.Lys1070Met
XM_005267069.3:c.3329A>T	XP_005267126.2:p.Lys1110Met
XM_011535984.1:c.2408A>T	XP_011534286.1:p.Lys803Met
XM_011535985.1:c.2228A>T	XP_011534287.1:p.Lys743Met
XM_011535986.1:c.1988A>T	XP_011534288.1:p.Lys663Met
XM_011535987.1:c.1607A>T	XP_011534289.1:p.Lys536Met
XM_011535988.1:c.470A>T	XP_011534290.1:p.Lys157Met
NM_001346813.1:c.3329A>T	NP_001333742.1:p.Lys1110Met
NM_001363725.1:c.1079A>T	NP_001350654.1:p.Lys360Met
XM_011535984.2:c.3539A>T	XP_011534286.2:p.Lys1180Met
XM_011535988.3:c.470A>T	XP_011534290.1:p.Lys157Met
XM_017011103.2:c.3440A>T	XP_016866592.1:p.Lys1147Met
XM_017011104.1:c.3410A>T	XP_016866593.1:p.Lys1137Met
XM_017011105.2:c.3380A>T	XP_016866594.1:p.Lys1127Met
XM_017011106.2:c.3251A>T	XP_016866595.1:p.Lys1084Met
XM_017011107.2:c.3230A>T	XP_016866596.1:p.Lys1077Met
XR_002956289.1:n.3622A>T
NM_001363725.2:c.1079A>T	NP_001350654.1:p.Lys360Met
NM_001371656.1:c.3458A>T	NP_001358585.1:p.Lys1153Met
NM_001374820.1:c.3458A>T	NP_001361749.1:p.Lys1153Met
NM_001374828.1:c.3578A>T MANE Select	NP_001361757.1:p.Lys1193Met
NM_017519.3:c.3419A>T	NP_059989.3:p.Lys1140Met