Canonical Allele Identifier: CA366234112

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510833T>A (hg19) ; chr6:g.157189699T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3818T>A	ENSP00000055163.8:p.Met1273Lys
ENST00000414678.8:c.3887T>A	ENSP00000412835.3:p.Met1296Lys
ENST00000637015.2:c.4106T>A	ENSP00000489729.2:p.Met1369Lys
ENST00000346085.10:c.3857T>A	ENSP00000344546.5:p.Met1286Lys
ENST00000350026.10:c.3569T>A	ENSP00000055163.7:p.Met1190Lys
ENST00000414678.7:c.2135T>A	ENSP00000412835.2:p.Met712Lys
ENST00000635849.1:c.1298T>A	ENSP00000490948.1:p.Met433Lys
ENST00000635957.1:c.932T>A	ENSP00000490385.1:p.Met311Lys
ENST00000636930.2:c.3977T>A MANE Select	ENSP00000490491.2:p.Met1326Lys
ENST00000636940.1:n.1974T>A
ENST00000637015.1:c.1345T>A
ENST00000637568.1:c.1259T>A
ENST00000637741.1:n.643T>A
ENST00000637810.1:c.1319T>A	ENSP00000489636.1:p.Met440Lys
ENST00000637904.1:c.1478T>A	ENSP00000490550.1:p.Met493Lys
ENST00000647938.1:c.3608T>A	ENSP00000498155.1:p.Met1203Lys
ENST00000346085.9:c.3608T>A	ENSP00000344546.4:p.Met1203Lys
ENST00000350026.9:c.3569T>A	ENSP00000055163.7:p.Met1190Lys
ENST00000414678.6:c.2135T>A	ENSP00000412835.2:p.Met712Lys
NM_017519.2:c.3569T>A	NP_059989.2:p.Met1190Lys
NM_020732.3:c.3608T>A	NP_065783.3:p.Met1203Lys
XM_005267069.3:c.3728T>A	XP_005267126.2:p.Met1243Lys
XM_011535984.1:c.2807T>A	XP_011534286.1:p.Met936Lys
XM_011535985.1:c.2627T>A	XP_011534287.1:p.Met876Lys
XM_011535986.1:c.2387T>A	XP_011534288.1:p.Met796Lys
XM_011535987.1:c.2006T>A	XP_011534289.1:p.Met669Lys
XM_011535988.1:c.869T>A	XP_011534290.1:p.Met290Lys
NM_001346813.1:c.3728T>A	NP_001333742.1:p.Met1243Lys
NM_001363725.1:c.1478T>A	NP_001350654.1:p.Met493Lys
XM_011535984.2:c.3938T>A	XP_011534286.2:p.Met1313Lys
XM_011535988.3:c.869T>A	XP_011534290.1:p.Met290Lys
XM_017011103.2:c.3839T>A	XP_016866592.1:p.Met1280Lys
XM_017011104.1:c.3809T>A	XP_016866593.1:p.Met1270Lys
XM_017011105.2:c.3779T>A	XP_016866594.1:p.Met1260Lys
XM_017011106.2:c.3650T>A	XP_016866595.1:p.Met1217Lys
XM_017011107.2:c.3629T>A	XP_016866596.1:p.Met1210Lys
XR_002956289.1:n.4021T>A
NM_001363725.2:c.1478T>A	NP_001350654.1:p.Met493Lys
NM_001371656.1:c.3857T>A	NP_001358585.1:p.Met1286Lys
NM_001374820.1:c.3857T>A	NP_001361749.1:p.Met1286Lys
NM_001374828.1:c.3977T>A MANE Select	NP_001361757.1:p.Met1326Lys
NM_017519.3:c.3818T>A	NP_059989.3:p.Met1273Lys