Canonical Allele Identifier: CA366234113

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2016057
• ClinVar RCV Id: RCV002851382
• MyVariant Identifiers: chr6:g.157510833T>C (hg19) ; chr6:g.157189699T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189699T>C , CM000668.2:g.157189699T>C	GRCh38
NC_000006.11:g.157510833T>C , CM000668.1:g.157510833T>C	GRCh37
NC_000006.10:g.157552525T>C	NCBI36
NG_032093.1:g.416770T>C
NG_032093.2:g.416770T>C
NG_066624.1:g.418674T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3818T>C	ENSP00000055163.8:p.Met1273Thr
ENST00000414678.8:c.3887T>C	ENSP00000412835.3:p.Met1296Thr
ENST00000637015.2:c.4106T>C	ENSP00000489729.2:p.Met1369Thr
ENST00000346085.10:c.3857T>C	ENSP00000344546.5:p.Met1286Thr
ENST00000350026.10:c.3569T>C	ENSP00000055163.7:p.Met1190Thr
ENST00000414678.7:c.2135T>C	ENSP00000412835.2:p.Met712Thr
ENST00000635849.1:c.1298T>C	ENSP00000490948.1:p.Met433Thr
ENST00000635957.1:c.932T>C	ENSP00000490385.1:p.Met311Thr
ENST00000636930.2:c.3977T>C MANE Select	ENSP00000490491.2:p.Met1326Thr
ENST00000636940.1:n.1974T>C
ENST00000637015.1:c.1345T>C
ENST00000637568.1:c.1259T>C
ENST00000637741.1:n.643T>C
ENST00000637810.1:c.1319T>C	ENSP00000489636.1:p.Met440Thr
ENST00000637904.1:c.1478T>C	ENSP00000490550.1:p.Met493Thr
ENST00000647938.1:c.3608T>C	ENSP00000498155.1:p.Met1203Thr
ENST00000346085.9:c.3608T>C	ENSP00000344546.4:p.Met1203Thr
ENST00000350026.9:c.3569T>C	ENSP00000055163.7:p.Met1190Thr
ENST00000414678.6:c.2135T>C	ENSP00000412835.2:p.Met712Thr
NM_017519.2:c.3569T>C	NP_059989.2:p.Met1190Thr
NM_020732.3:c.3608T>C	NP_065783.3:p.Met1203Thr
XM_005267069.3:c.3728T>C	XP_005267126.2:p.Met1243Thr
XM_011535984.1:c.2807T>C	XP_011534286.1:p.Met936Thr
XM_011535985.1:c.2627T>C	XP_011534287.1:p.Met876Thr
XM_011535986.1:c.2387T>C	XP_011534288.1:p.Met796Thr
XM_011535987.1:c.2006T>C	XP_011534289.1:p.Met669Thr
XM_011535988.1:c.869T>C	XP_011534290.1:p.Met290Thr
NM_001346813.1:c.3728T>C	NP_001333742.1:p.Met1243Thr
NM_001363725.1:c.1478T>C	NP_001350654.1:p.Met493Thr
XM_011535984.2:c.3938T>C	XP_011534286.2:p.Met1313Thr
XM_011535988.3:c.869T>C	XP_011534290.1:p.Met290Thr
XM_017011103.2:c.3839T>C	XP_016866592.1:p.Met1280Thr
XM_017011104.1:c.3809T>C	XP_016866593.1:p.Met1270Thr
XM_017011105.2:c.3779T>C	XP_016866594.1:p.Met1260Thr
XM_017011106.2:c.3650T>C	XP_016866595.1:p.Met1217Thr
XM_017011107.2:c.3629T>C	XP_016866596.1:p.Met1210Thr
XR_002956289.1:n.4021T>C
NM_001363725.2:c.1478T>C	NP_001350654.1:p.Met493Thr
NM_001371656.1:c.3857T>C	NP_001358585.1:p.Met1286Thr
NM_001374820.1:c.3857T>C	NP_001361749.1:p.Met1286Thr
NM_001374828.1:c.3977T>C MANE Select	NP_001361757.1:p.Met1326Thr
NM_017519.3:c.3818T>C	NP_059989.3:p.Met1273Thr