Canonical Allele Identifier: CA366234115

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510834G>C (hg19) ; chr6:g.157189700G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189700G>C , CM000668.2:g.157189700G>C	GRCh38
NC_000006.11:g.157510834G>C , CM000668.1:g.157510834G>C	GRCh37
NC_000006.10:g.157552526G>C	NCBI36
NG_032093.1:g.416771G>C
NG_032093.2:g.416771G>C
NG_066624.1:g.418675G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3819G>C	ENSP00000055163.8:p.Met1273Ile
ENST00000414678.8:c.3888G>C	ENSP00000412835.3:p.Met1296Ile
ENST00000637015.2:c.4107G>C	ENSP00000489729.2:p.Met1369Ile
ENST00000346085.10:c.3858G>C	ENSP00000344546.5:p.Met1286Ile
ENST00000350026.10:c.3570G>C	ENSP00000055163.7:p.Met1190Ile
ENST00000414678.7:c.2136G>C	ENSP00000412835.2:p.Met712Ile
ENST00000635849.1:c.1299G>C	ENSP00000490948.1:p.Met433Ile
ENST00000635957.1:c.933G>C	ENSP00000490385.1:p.Met311Ile
ENST00000636930.2:c.3978G>C MANE Select	ENSP00000490491.2:p.Met1326Ile
ENST00000636940.1:n.1975G>C
ENST00000637015.1:c.1346G>C
ENST00000637568.1:c.1260G>C
ENST00000637741.1:n.644G>C
ENST00000637810.1:c.1320G>C	ENSP00000489636.1:p.Met440Ile
ENST00000637904.1:c.1479G>C	ENSP00000490550.1:p.Met493Ile
ENST00000647938.1:c.3609G>C	ENSP00000498155.1:p.Met1203Ile
ENST00000346085.9:c.3609G>C	ENSP00000344546.4:p.Met1203Ile
ENST00000350026.9:c.3570G>C	ENSP00000055163.7:p.Met1190Ile
ENST00000414678.6:c.2136G>C	ENSP00000412835.2:p.Met712Ile
NM_017519.2:c.3570G>C	NP_059989.2:p.Met1190Ile
NM_020732.3:c.3609G>C	NP_065783.3:p.Met1203Ile
XM_005267069.3:c.3729G>C	XP_005267126.2:p.Met1243Ile
XM_011535984.1:c.2808G>C	XP_011534286.1:p.Met936Ile
XM_011535985.1:c.2628G>C	XP_011534287.1:p.Met876Ile
XM_011535986.1:c.2388G>C	XP_011534288.1:p.Met796Ile
XM_011535987.1:c.2007G>C	XP_011534289.1:p.Met669Ile
XM_011535988.1:c.870G>C	XP_011534290.1:p.Met290Ile
NM_001346813.1:c.3729G>C	NP_001333742.1:p.Met1243Ile
NM_001363725.1:c.1479G>C	NP_001350654.1:p.Met493Ile
XM_011535984.2:c.3939G>C	XP_011534286.2:p.Met1313Ile
XM_011535988.3:c.870G>C	XP_011534290.1:p.Met290Ile
XM_017011103.2:c.3840G>C	XP_016866592.1:p.Met1280Ile
XM_017011104.1:c.3810G>C	XP_016866593.1:p.Met1270Ile
XM_017011105.2:c.3780G>C	XP_016866594.1:p.Met1260Ile
XM_017011106.2:c.3651G>C	XP_016866595.1:p.Met1217Ile
XM_017011107.2:c.3630G>C	XP_016866596.1:p.Met1210Ile
XR_002956289.1:n.4022G>C
NM_001363725.2:c.1479G>C	NP_001350654.1:p.Met493Ile
NM_001371656.1:c.3858G>C	NP_001358585.1:p.Met1286Ile
NM_001374820.1:c.3858G>C	NP_001361749.1:p.Met1286Ile
NM_001374828.1:c.3978G>C MANE Select	NP_001361757.1:p.Met1326Ile
NM_017519.3:c.3819G>C	NP_059989.3:p.Met1273Ile