Canonical Allele Identifier: CA366388963

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469926G>T (hg19) ; chr6:g.157148792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148792G>T , CM000668.2:g.157148792G>T	GRCh38
NC_000006.11:g.157469926G>T , CM000668.1:g.157469926G>T	GRCh37
NC_000006.10:g.157511618G>T	NCBI36
NG_032093.1:g.375863G>T
NG_032093.2:g.375863G>T
NG_066624.1:g.377767G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2930G>T	ENSP00000055163.8:p.Arg977Ile
ENST00000414678.8:c.2840G>T	ENSP00000412835.3:p.Arg947Ile
ENST00000637015.2:c.2930G>T	ENSP00000489729.2:p.Arg977Ile
ENST00000319584.11:c.944G>T	ENSP00000313006.7:p.Arg315Ile
ENST00000346085.10:c.2969G>T	ENSP00000344546.5:p.Arg990Ile
ENST00000350026.10:c.2681G>T	ENSP00000055163.7:p.Arg894Ile
ENST00000414678.7:c.1088G>T	ENSP00000412835.2:p.Arg363Ile
ENST00000452544.2:n.831G>T
ENST00000635849.1:c.251G>T	ENSP00000490948.1:p.Arg84Ile
ENST00000636426.1:n.64G>T
ENST00000636930.2:c.2930G>T MANE Select	ENSP00000490491.2:p.Arg977Ile
ENST00000637015.1:c.169G>T
ENST00000637810.1:c.431G>T	ENSP00000489636.1:p.Arg144Ile
ENST00000637904.1:c.431G>T	ENSP00000490550.1:p.Arg144Ile
ENST00000647938.1:c.2720G>T	ENSP00000498155.1:p.Arg907Ile
ENST00000674190.1:n.1679G>T
ENST00000319584.10:c.947G>T	ENSP00000313006.6:p.Arg316Ile
ENST00000346085.9:c.2720G>T	ENSP00000344546.4:p.Arg907Ile
ENST00000350026.9:c.2681G>T	ENSP00000055163.7:p.Arg894Ile
ENST00000414678.6:c.1088G>T	ENSP00000412835.2:p.Arg363Ile
ENST00000452544.1:n.777G>T
ENST00000478761.3:c.3G>T
NM_017519.2:c.2681G>T	NP_059989.2:p.Arg894Ile
NM_020732.3:c.2720G>T	NP_065783.3:p.Arg907Ile
XM_005267069.3:c.2681G>T	XP_005267126.2:p.Arg894Ile
XM_011535984.1:c.1631G>T	XP_011534286.1:p.Arg544Ile
XM_011535985.1:c.1451G>T	XP_011534287.1:p.Arg484Ile
XM_011535986.1:c.1211G>T	XP_011534288.1:p.Arg404Ile
XM_011535987.1:c.830G>T	XP_011534289.1:p.Arg277Ile
XM_011535988.1:c.-20+15585G>T	XP_011534290.1:n.-20+15585G>T
NM_001346813.1:c.2681G>T	NP_001333742.1:p.Arg894Ile
NM_001363725.1:c.431G>T	NP_001350654.1:p.Arg144Ile
XM_011535984.2:c.2762G>T	XP_011534286.2:p.Arg921Ile
XM_011535988.3:c.-20+15585G>T	XP_011534290.1:n.-20+15585G>T
XM_017011103.2:c.2762G>T	XP_016866592.1:p.Arg921Ile
XM_017011104.1:c.2762G>T	XP_016866593.1:p.Arg921Ile
XM_017011105.2:c.2762G>T	XP_016866594.1:p.Arg921Ile
XM_017011106.2:c.2762G>T	XP_016866595.1:p.Arg921Ile
XM_017011107.2:c.2582G>T	XP_016866596.1:p.Arg861Ile
XR_002956289.1:n.2845G>T
NM_001363725.2:c.431G>T	NP_001350654.1:p.Arg144Ile
NM_001371656.1:c.2969G>T	NP_001358585.1:p.Arg990Ile
NM_001374820.1:c.2969G>T	NP_001361749.1:p.Arg990Ile
NM_001374828.1:c.2930G>T MANE Select	NP_001361757.1:p.Arg977Ile
NM_017519.3:c.2930G>T	NP_059989.3:p.Arg977Ile