Canonical Allele Identifier: CA366388966

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469927A>T (hg19) ; chr6:g.157148793A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148793A>T , CM000668.2:g.157148793A>T	GRCh38
NC_000006.11:g.157469927A>T , CM000668.1:g.157469927A>T	GRCh37
NC_000006.10:g.157511619A>T	NCBI36
NG_032093.1:g.375864A>T
NG_032093.2:g.375864A>T
NG_066624.1:g.377768A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2931A>T	ENSP00000055163.8:p.Arg977Ser
ENST00000414678.8:c.2841A>T	ENSP00000412835.3:p.Arg947Ser
ENST00000637015.2:c.2931A>T	ENSP00000489729.2:p.Arg977Ser
ENST00000319584.11:c.945A>T	ENSP00000313006.7:p.Arg315Ser
ENST00000346085.10:c.2970A>T	ENSP00000344546.5:p.Arg990Ser
ENST00000350026.10:c.2682A>T	ENSP00000055163.7:p.Arg894Ser
ENST00000414678.7:c.1089A>T	ENSP00000412835.2:p.Arg363Ser
ENST00000452544.2:n.832A>T
ENST00000635849.1:c.252A>T	ENSP00000490948.1:p.Arg84Ser
ENST00000636426.1:n.65A>T
ENST00000636930.2:c.2931A>T MANE Select	ENSP00000490491.2:p.Arg977Ser
ENST00000637015.1:c.170A>T
ENST00000637810.1:c.432A>T	ENSP00000489636.1:p.Arg144Ser
ENST00000637904.1:c.432A>T	ENSP00000490550.1:p.Arg144Ser
ENST00000647938.1:c.2721A>T	ENSP00000498155.1:p.Arg907Ser
ENST00000674190.1:n.1680A>T
ENST00000319584.10:c.948A>T	ENSP00000313006.6:p.Arg316Ser
ENST00000346085.9:c.2721A>T	ENSP00000344546.4:p.Arg907Ser
ENST00000350026.9:c.2682A>T	ENSP00000055163.7:p.Arg894Ser
ENST00000414678.6:c.1089A>T	ENSP00000412835.2:p.Arg363Ser
ENST00000452544.1:n.778A>T
ENST00000478761.3:c.4A>T
NM_017519.2:c.2682A>T	NP_059989.2:p.Arg894Ser
NM_020732.3:c.2721A>T	NP_065783.3:p.Arg907Ser
XM_005267069.3:c.2682A>T	XP_005267126.2:p.Arg894Ser
XM_011535984.1:c.1632A>T	XP_011534286.1:p.Arg544Ser
XM_011535985.1:c.1452A>T	XP_011534287.1:p.Arg484Ser
XM_011535986.1:c.1212A>T	XP_011534288.1:p.Arg404Ser
XM_011535987.1:c.831A>T	XP_011534289.1:p.Arg277Ser
XM_011535988.1:c.-20+15586A>T	XP_011534290.1:n.-20+15586A>T
NM_001346813.1:c.2682A>T	NP_001333742.1:p.Arg894Ser
NM_001363725.1:c.432A>T	NP_001350654.1:p.Arg144Ser
XM_011535984.2:c.2763A>T	XP_011534286.2:p.Arg921Ser
XM_011535988.3:c.-20+15586A>T	XP_011534290.1:n.-20+15586A>T
XM_017011103.2:c.2763A>T	XP_016866592.1:p.Arg921Ser
XM_017011104.1:c.2763A>T	XP_016866593.1:p.Arg921Ser
XM_017011105.2:c.2763A>T	XP_016866594.1:p.Arg921Ser
XM_017011106.2:c.2763A>T	XP_016866595.1:p.Arg921Ser
XM_017011107.2:c.2583A>T	XP_016866596.1:p.Arg861Ser
XR_002956289.1:n.2846A>T
NM_001363725.2:c.432A>T	NP_001350654.1:p.Arg144Ser
NM_001371656.1:c.2970A>T	NP_001358585.1:p.Arg990Ser
NM_001374820.1:c.2970A>T	NP_001361749.1:p.Arg990Ser
NM_001374828.1:c.2931A>T MANE Select	NP_001361757.1:p.Arg977Ser
NM_017519.3:c.2931A>T	NP_059989.3:p.Arg977Ser