Canonical Allele Identifier: CA366380946

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157222643G>T (hg19) ; chr6:g.156901509G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901509G>T , CM000668.2:g.156901509G>T	GRCh38
NC_000006.11:g.157222643G>T , CM000668.1:g.157222643G>T	GRCh37
NC_000006.10:g.157264335G>T	NCBI36
NG_032093.1:g.128580G>T
NG_032093.2:g.128580G>T
NG_066624.1:g.130484G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2120G>T	ENSP00000055163.8:p.Arg707Met
ENST00000414678.8:c.2120G>T	ENSP00000412835.3:p.Arg707Met
ENST00000637015.2:c.2120G>T	ENSP00000489729.2:p.Arg707Met
ENST00000319584.11:c.134G>T	ENSP00000313006.7:p.Arg45Met
ENST00000346085.10:c.2159G>T	ENSP00000344546.5:p.Arg720Met
ENST00000350026.10:c.1871G>T	ENSP00000055163.7:p.Arg624Met
ENST00000414678.7:c.368G>T	ENSP00000412835.2:p.Arg123Met
ENST00000636205.1:n.183G>T
ENST00000636748.1:c.401G>T	ENSP00000489917.1:p.Arg134Met
ENST00000636930.2:c.2120G>T MANE Select	ENSP00000490491.2:p.Arg707Met
ENST00000637532.1:c.146G>T	ENSP00000490420.1:p.Arg49Met
ENST00000638000.1:c.337G>T
ENST00000647938.1:c.1910G>T	ENSP00000498155.1:p.Arg637Met
ENST00000674190.1:n.827G>T
ENST00000674298.1:c.1860G>T
ENST00000319584.10:c.137G>T	ENSP00000313006.6:p.Arg46Met
ENST00000346085.9:c.1910G>T	ENSP00000344546.4:p.Arg637Met
ENST00000350026.9:c.1871G>T	ENSP00000055163.7:p.Arg624Met
ENST00000414678.6:c.368G>T	ENSP00000412835.2:p.Arg123Met
NM_017519.2:c.1871G>T	NP_059989.2:p.Arg624Met
NM_020732.3:c.1910G>T	NP_065783.3:p.Arg637Met
XM_005267069.3:c.1871G>T	XP_005267126.2:p.Arg624Met
XM_011535984.1:c.779G>T	XP_011534286.1:p.Arg260Met
XM_011535985.1:c.779G>T	XP_011534287.1:p.Arg260Met
XM_011535986.1:c.359G>T	XP_011534288.1:p.Arg120Met
NM_001346813.1:c.1871G>T	NP_001333742.1:p.Arg624Met
XM_011535984.2:c.1910G>T	XP_011534286.2:p.Arg637Met
XM_017011103.2:c.1910G>T	XP_016866592.1:p.Arg637Met
XM_017011104.1:c.1910G>T	XP_016866593.1:p.Arg637Met
XM_017011105.2:c.1910G>T	XP_016866594.1:p.Arg637Met
XM_017011106.2:c.1910G>T	XP_016866595.1:p.Arg637Met
XM_017011107.2:c.1910G>T	XP_016866596.1:p.Arg637Met
XR_002956289.1:n.1993G>T
NM_001371656.1:c.2159G>T	NP_001358585.1:p.Arg720Met
NM_001374820.1:c.2159G>T	NP_001361749.1:p.Arg720Met
NM_001374828.1:c.2120G>T MANE Select	NP_001361757.1:p.Arg707Met
NM_017519.3:c.2120G>T	NP_059989.3:p.Arg707Met