Canonical Allele Identifier: CA366234008

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554232914
• MyVariant Identifiers: chr6:g.157510784G>T (hg19) ; chr6:g.157189650G>T (hg38)
• PubMed: PMID:28263302

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189650G>T , CM000668.2:g.157189650G>T	GRCh38
NC_000006.11:g.157510784G>T , CM000668.1:g.157510784G>T	GRCh37
NC_000006.10:g.157552476G>T	NCBI36
NG_032093.1:g.416721G>T
NG_032093.2:g.416721G>T
NG_066624.1:g.418625G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3769G>T	ENSP00000055163.8:p.Gly1257Ter
ENST00000414678.8:c.3838G>T	ENSP00000412835.3:p.Gly1280Ter
ENST00000637015.2:c.4057G>T	ENSP00000489729.2:p.Gly1353Ter
ENST00000346085.10:c.3808G>T	ENSP00000344546.5:p.Gly1270Ter
ENST00000350026.10:c.3520G>T	ENSP00000055163.7:p.Gly1174Ter
ENST00000414678.7:c.2086G>T	ENSP00000412835.2:p.Gly696Ter
ENST00000635849.1:c.1249G>T	ENSP00000490948.1:p.Gly417Ter
ENST00000635957.1:c.883G>T	ENSP00000490385.1:p.Gly295Ter
ENST00000636930.2:c.3928G>T MANE Select	ENSP00000490491.2:p.Gly1310Ter
ENST00000636940.1:n.1925G>T
ENST00000637015.1:c.1296G>T
ENST00000637568.1:c.1210G>T
ENST00000637741.1:n.594G>T
ENST00000637810.1:c.1270G>T	ENSP00000489636.1:p.Gly424Ter
ENST00000637904.1:c.1429G>T	ENSP00000490550.1:p.Gly477Ter
ENST00000647938.1:c.3559G>T	ENSP00000498155.1:p.Gly1187Ter
ENST00000346085.9:c.3559G>T	ENSP00000344546.4:p.Gly1187Ter
ENST00000350026.9:c.3520G>T	ENSP00000055163.7:p.Gly1174Ter
ENST00000414678.6:c.2086G>T	ENSP00000412835.2:p.Gly696Ter
NM_017519.2:c.3520G>T	NP_059989.2:p.Gly1174Ter
NM_020732.3:c.3559G>T	NP_065783.3:p.Gly1187Ter
XM_005267069.3:c.3679G>T	XP_005267126.2:p.Gly1227Ter
XM_011535984.1:c.2758G>T	XP_011534286.1:p.Gly920Ter
XM_011535985.1:c.2578G>T	XP_011534287.1:p.Gly860Ter
XM_011535986.1:c.2338G>T	XP_011534288.1:p.Gly780Ter
XM_011535987.1:c.1957G>T	XP_011534289.1:p.Gly653Ter
XM_011535988.1:c.820G>T	XP_011534290.1:p.Gly274Ter
NM_001346813.1:c.3679G>T	NP_001333742.1:p.Gly1227Ter
NM_001363725.1:c.1429G>T	NP_001350654.1:p.Gly477Ter
XM_011535984.2:c.3889G>T	XP_011534286.2:p.Gly1297Ter
XM_011535988.3:c.820G>T	XP_011534290.1:p.Gly274Ter
XM_017011103.2:c.3790G>T	XP_016866592.1:p.Gly1264Ter
XM_017011104.1:c.3760G>T	XP_016866593.1:p.Gly1254Ter
XM_017011105.2:c.3730G>T	XP_016866594.1:p.Gly1244Ter
XM_017011106.2:c.3601G>T	XP_016866595.1:p.Gly1201Ter
XM_017011107.2:c.3580G>T	XP_016866596.1:p.Gly1194Ter
XR_002956289.1:n.3972G>T
NM_001363725.2:c.1429G>T	NP_001350654.1:p.Gly477Ter
NM_001371656.1:c.3808G>T	NP_001358585.1:p.Gly1270Ter
NM_001374820.1:c.3808G>T	NP_001361749.1:p.Gly1270Ter
NM_001374828.1:c.3928G>T MANE Select	NP_001361757.1:p.Gly1310Ter
NM_017519.3:c.3769G>T	NP_059989.3:p.Gly1257Ter