Canonical Allele Identifier: CA366389169

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470019T>A (hg19) ; chr6:g.157148885T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148885T>A , CM000668.2:g.157148885T>A	GRCh38
NC_000006.11:g.157470019T>A , CM000668.1:g.157470019T>A	GRCh37
NC_000006.10:g.157511711T>A	NCBI36
NG_032093.1:g.375956T>A
NG_032093.2:g.375956T>A
NG_066624.1:g.377860T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3023T>A	ENSP00000055163.8:p.Val1008Glu
ENST00000414678.8:c.2933T>A	ENSP00000412835.3:p.Val978Glu
ENST00000637015.2:c.3023T>A	ENSP00000489729.2:p.Val1008Glu
ENST00000319584.11:c.1037T>A	ENSP00000313006.7:p.Val346Glu
ENST00000346085.10:c.3062T>A	ENSP00000344546.5:p.Val1021Glu
ENST00000350026.10:c.2774T>A	ENSP00000055163.7:p.Val925Glu
ENST00000414678.7:c.1181T>A	ENSP00000412835.2:p.Val394Glu
ENST00000452544.2:n.924T>A
ENST00000635849.1:c.344T>A	ENSP00000490948.1:p.Val115Glu
ENST00000636426.1:n.157T>A
ENST00000636930.2:c.3023T>A MANE Select	ENSP00000490491.2:p.Val1008Glu
ENST00000637015.1:c.262T>A
ENST00000637568.1:c.66T>A
ENST00000637810.1:c.524T>A	ENSP00000489636.1:p.Val175Glu
ENST00000637904.1:c.524T>A	ENSP00000490550.1:p.Val175Glu
ENST00000647938.1:c.2813T>A	ENSP00000498155.1:p.Val938Glu
ENST00000674190.1:n.1772T>A
ENST00000319584.10:c.1040T>A	ENSP00000313006.6:p.Val347Glu
ENST00000346085.9:c.2813T>A	ENSP00000344546.4:p.Val938Glu
ENST00000350026.9:c.2774T>A	ENSP00000055163.7:p.Val925Glu
ENST00000414678.6:c.1181T>A	ENSP00000412835.2:p.Val394Glu
ENST00000452544.1:n.870T>A
ENST00000478761.3:c.96T>A
NM_017519.2:c.2774T>A	NP_059989.2:p.Val925Glu
NM_020732.3:c.2813T>A	NP_065783.3:p.Val938Glu
XM_005267069.3:c.2774T>A	XP_005267126.2:p.Val925Glu
XM_011535984.1:c.1724T>A	XP_011534286.1:p.Val575Glu
XM_011535985.1:c.1544T>A	XP_011534287.1:p.Val515Glu
XM_011535986.1:c.1304T>A	XP_011534288.1:p.Val435Glu
XM_011535987.1:c.923T>A	XP_011534289.1:p.Val308Glu
XM_011535988.1:c.-20+15678T>A	XP_011534290.1:n.-20+15678T>A
NM_001346813.1:c.2774T>A	NP_001333742.1:p.Val925Glu
NM_001363725.1:c.524T>A	NP_001350654.1:p.Val175Glu
XM_011535984.2:c.2855T>A	XP_011534286.2:p.Val952Glu
XM_011535988.3:c.-20+15678T>A	XP_011534290.1:n.-20+15678T>A
XM_017011103.2:c.2855T>A	XP_016866592.1:p.Val952Glu
XM_017011104.1:c.2855T>A	XP_016866593.1:p.Val952Glu
XM_017011105.2:c.2855T>A	XP_016866594.1:p.Val952Glu
XM_017011106.2:c.2855T>A	XP_016866595.1:p.Val952Glu
XM_017011107.2:c.2675T>A	XP_016866596.1:p.Val892Glu
XR_002956289.1:n.2938T>A
NM_001363725.2:c.524T>A	NP_001350654.1:p.Val175Glu
NM_001371656.1:c.3062T>A	NP_001358585.1:p.Val1021Glu
NM_001374820.1:c.3062T>A	NP_001361749.1:p.Val1021Glu
NM_001374828.1:c.3023T>A MANE Select	NP_001361757.1:p.Val1008Glu
NM_017519.3:c.3023T>A	NP_059989.3:p.Val1008Glu