Canonical Allele Identifier: CA366235115

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190090-T-G
• MyVariant Identifiers: chr6:g.157511224T>G (hg19) ; chr6:g.157190090T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190090T>G , CM000668.2:g.157190090T>G	GRCh38
NC_000006.11:g.157511224T>G , CM000668.1:g.157511224T>G	GRCh37
NC_000006.10:g.157552916T>G	NCBI36
NG_032093.1:g.417161T>G
NG_032093.2:g.417161T>G
NG_066624.1:g.419065T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3952T>G	ENSP00000055163.8:p.Phe1318Val
ENST00000414678.8:c.4021T>G	ENSP00000412835.3:p.Phe1341Val
ENST00000637015.2:c.4240T>G	ENSP00000489729.2:p.Phe1414Val
ENST00000346085.10:c.3991T>G	ENSP00000344546.5:p.Phe1331Val
ENST00000350026.10:c.3703T>G	ENSP00000055163.7:p.Phe1235Val
ENST00000414678.7:c.2269T>G	ENSP00000412835.2:p.Phe757Val
ENST00000635849.1:c.1432T>G	ENSP00000490948.1:p.Phe478Val
ENST00000635957.1:c.1063T>G	ENSP00000490385.1:p.Phe355Val
ENST00000636930.2:c.4111T>G MANE Select	ENSP00000490491.2:p.Phe1371Val
ENST00000636940.1:n.2108T>G
ENST00000637015.1:c.1479T>G
ENST00000637568.1:c.1393T>G
ENST00000637741.1:n.777T>G
ENST00000637810.1:c.1453T>G	ENSP00000489636.1:p.Phe485Val
ENST00000637904.1:c.1612T>G	ENSP00000490550.1:p.Phe538Val
ENST00000647938.1:c.3742T>G	ENSP00000498155.1:p.Phe1248Val
ENST00000346085.9:c.3742T>G	ENSP00000344546.4:p.Phe1248Val
ENST00000350026.9:c.3703T>G	ENSP00000055163.7:p.Phe1235Val
ENST00000414678.6:c.2269T>G	ENSP00000412835.2:p.Phe757Val
NM_017519.2:c.3703T>G	NP_059989.2:p.Phe1235Val
NM_020732.3:c.3742T>G	NP_065783.3:p.Phe1248Val
XM_005267069.3:c.3862T>G	XP_005267126.2:p.Phe1288Val
XM_011535984.1:c.2941T>G	XP_011534286.1:p.Phe981Val
XM_011535985.1:c.2761T>G	XP_011534287.1:p.Phe921Val
XM_011535986.1:c.2521T>G	XP_011534288.1:p.Phe841Val
XM_011535987.1:c.2140T>G	XP_011534289.1:p.Phe714Val
XM_011535988.1:c.1003T>G	XP_011534290.1:p.Phe335Val
NM_001346813.1:c.3862T>G	NP_001333742.1:p.Phe1288Val
NM_001363725.1:c.1612T>G	NP_001350654.1:p.Phe538Val
XM_011535984.2:c.4072T>G	XP_011534286.2:p.Phe1358Val
XM_011535988.3:c.1003T>G	XP_011534290.1:p.Phe335Val
XM_017011103.2:c.3973T>G	XP_016866592.1:p.Phe1325Val
XM_017011104.1:c.3943T>G	XP_016866593.1:p.Phe1315Val
XM_017011105.2:c.3913T>G	XP_016866594.1:p.Phe1305Val
XM_017011106.2:c.3784T>G	XP_016866595.1:p.Phe1262Val
XM_017011107.2:c.3763T>G	XP_016866596.1:p.Phe1255Val
XR_002956289.1:n.4155T>G
NM_001363725.2:c.1612T>G	NP_001350654.1:p.Phe538Val
NM_001371656.1:c.3991T>G	NP_001358585.1:p.Phe1331Val
NM_001374820.1:c.3991T>G	NP_001361749.1:p.Phe1331Val
NM_001374828.1:c.4111T>G MANE Select	NP_001361757.1:p.Phe1371Val
NM_017519.3:c.3952T>G	NP_059989.3:p.Phe1318Val