Canonical Allele Identifier: CA366389047

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469962G>C (hg19) ; chr6:g.157148828G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148828G>C , CM000668.2:g.157148828G>C	GRCh38
NC_000006.11:g.157469962G>C , CM000668.1:g.157469962G>C	GRCh37
NC_000006.10:g.157511654G>C	NCBI36
NG_032093.1:g.375899G>C
NG_032093.2:g.375899G>C
NG_066624.1:g.377803G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2966G>C	ENSP00000055163.8:p.Ser989Thr
ENST00000414678.8:c.2876G>C	ENSP00000412835.3:p.Ser959Thr
ENST00000637015.2:c.2966G>C	ENSP00000489729.2:p.Ser989Thr
ENST00000319584.11:c.980G>C	ENSP00000313006.7:p.Ser327Thr
ENST00000346085.10:c.3005G>C	ENSP00000344546.5:p.Ser1002Thr
ENST00000350026.10:c.2717G>C	ENSP00000055163.7:p.Ser906Thr
ENST00000414678.7:c.1124G>C	ENSP00000412835.2:p.Ser375Thr
ENST00000452544.2:n.867G>C
ENST00000635849.1:c.287G>C	ENSP00000490948.1:p.Ser96Thr
ENST00000636426.1:n.100G>C
ENST00000636930.2:c.2966G>C MANE Select	ENSP00000490491.2:p.Ser989Thr
ENST00000637015.1:c.205G>C
ENST00000637568.1:c.9G>C
ENST00000637810.1:c.467G>C	ENSP00000489636.1:p.Ser156Thr
ENST00000637904.1:c.467G>C	ENSP00000490550.1:p.Ser156Thr
ENST00000647938.1:c.2756G>C	ENSP00000498155.1:p.Ser919Thr
ENST00000674190.1:n.1715G>C
ENST00000319584.10:c.983G>C	ENSP00000313006.6:p.Ser328Thr
ENST00000346085.9:c.2756G>C	ENSP00000344546.4:p.Ser919Thr
ENST00000350026.9:c.2717G>C	ENSP00000055163.7:p.Ser906Thr
ENST00000414678.6:c.1124G>C	ENSP00000412835.2:p.Ser375Thr
ENST00000452544.1:n.813G>C
ENST00000478761.3:c.39G>C
NM_017519.2:c.2717G>C	NP_059989.2:p.Ser906Thr
NM_020732.3:c.2756G>C	NP_065783.3:p.Ser919Thr
XM_005267069.3:c.2717G>C	XP_005267126.2:p.Ser906Thr
XM_011535984.1:c.1667G>C	XP_011534286.1:p.Ser556Thr
XM_011535985.1:c.1487G>C	XP_011534287.1:p.Ser496Thr
XM_011535986.1:c.1247G>C	XP_011534288.1:p.Ser416Thr
XM_011535987.1:c.866G>C	XP_011534289.1:p.Ser289Thr
XM_011535988.1:c.-20+15621G>C	XP_011534290.1:n.-20+15621G>C
NM_001346813.1:c.2717G>C	NP_001333742.1:p.Ser906Thr
NM_001363725.1:c.467G>C	NP_001350654.1:p.Ser156Thr
XM_011535984.2:c.2798G>C	XP_011534286.2:p.Ser933Thr
XM_011535988.3:c.-20+15621G>C	XP_011534290.1:n.-20+15621G>C
XM_017011103.2:c.2798G>C	XP_016866592.1:p.Ser933Thr
XM_017011104.1:c.2798G>C	XP_016866593.1:p.Ser933Thr
XM_017011105.2:c.2798G>C	XP_016866594.1:p.Ser933Thr
XM_017011106.2:c.2798G>C	XP_016866595.1:p.Ser933Thr
XM_017011107.2:c.2618G>C	XP_016866596.1:p.Ser873Thr
XR_002956289.1:n.2881G>C
NM_001363725.2:c.467G>C	NP_001350654.1:p.Ser156Thr
NM_001371656.1:c.3005G>C	NP_001358585.1:p.Ser1002Thr
NM_001374820.1:c.3005G>C	NP_001361749.1:p.Ser1002Thr
NM_001374828.1:c.2966G>C MANE Select	NP_001361757.1:p.Ser989Thr
NM_017519.3:c.2966G>C	NP_059989.3:p.Ser989Thr