Canonical Allele Identifier: CA366235256

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511234G>C (hg19) ; chr6:g.157190100G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190100G>C , CM000668.2:g.157190100G>C	GRCh38
NC_000006.11:g.157511234G>C , CM000668.1:g.157511234G>C	GRCh37
NC_000006.10:g.157552926G>C	NCBI36
NG_032093.1:g.417171G>C
NG_032093.2:g.417171G>C
NG_066624.1:g.419075G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3962G>C	ENSP00000055163.8:p.Arg1321Pro
ENST00000414678.8:c.4031G>C	ENSP00000412835.3:p.Arg1344Pro
ENST00000637015.2:c.4250G>C	ENSP00000489729.2:p.Arg1417Pro
ENST00000346085.10:c.4001G>C	ENSP00000344546.5:p.Arg1334Pro
ENST00000350026.10:c.3713G>C	ENSP00000055163.7:p.Arg1238Pro
ENST00000414678.7:c.2279G>C	ENSP00000412835.2:p.Arg760Pro
ENST00000635849.1:c.1442G>C	ENSP00000490948.1:p.Arg481Pro
ENST00000635957.1:c.1073G>C	ENSP00000490385.1:p.Arg358Pro
ENST00000636930.2:c.4121G>C MANE Select	ENSP00000490491.2:p.Arg1374Pro
ENST00000636940.1:n.2118G>C
ENST00000637015.1:c.1489G>C
ENST00000637568.1:c.1403G>C
ENST00000637741.1:n.787G>C
ENST00000637810.1:c.1463G>C	ENSP00000489636.1:p.Arg488Pro
ENST00000637904.1:c.1622G>C	ENSP00000490550.1:p.Arg541Pro
ENST00000647938.1:c.3752G>C	ENSP00000498155.1:p.Arg1251Pro
ENST00000346085.9:c.3752G>C	ENSP00000344546.4:p.Arg1251Pro
ENST00000350026.9:c.3713G>C	ENSP00000055163.7:p.Arg1238Pro
ENST00000414678.6:c.2279G>C	ENSP00000412835.2:p.Arg760Pro
NM_017519.2:c.3713G>C	NP_059989.2:p.Arg1238Pro
NM_020732.3:c.3752G>C	NP_065783.3:p.Arg1251Pro
XM_005267069.3:c.3872G>C	XP_005267126.2:p.Arg1291Pro
XM_011535984.1:c.2951G>C	XP_011534286.1:p.Arg984Pro
XM_011535985.1:c.2771G>C	XP_011534287.1:p.Arg924Pro
XM_011535986.1:c.2531G>C	XP_011534288.1:p.Arg844Pro
XM_011535987.1:c.2150G>C	XP_011534289.1:p.Arg717Pro
XM_011535988.1:c.1013G>C	XP_011534290.1:p.Arg338Pro
NM_001346813.1:c.3872G>C	NP_001333742.1:p.Arg1291Pro
NM_001363725.1:c.1622G>C	NP_001350654.1:p.Arg541Pro
XM_011535984.2:c.4082G>C	XP_011534286.2:p.Arg1361Pro
XM_011535988.3:c.1013G>C	XP_011534290.1:p.Arg338Pro
XM_017011103.2:c.3983G>C	XP_016866592.1:p.Arg1328Pro
XM_017011104.1:c.3953G>C	XP_016866593.1:p.Arg1318Pro
XM_017011105.2:c.3923G>C	XP_016866594.1:p.Arg1308Pro
XM_017011106.2:c.3794G>C	XP_016866595.1:p.Arg1265Pro
XM_017011107.2:c.3773G>C	XP_016866596.1:p.Arg1258Pro
XR_002956289.1:n.4165G>C
NM_001363725.2:c.1622G>C	NP_001350654.1:p.Arg541Pro
NM_001371656.1:c.4001G>C	NP_001358585.1:p.Arg1334Pro
NM_001374820.1:c.4001G>C	NP_001361749.1:p.Arg1334Pro
NM_001374828.1:c.4121G>C MANE Select	NP_001361757.1:p.Arg1374Pro
NM_017519.3:c.3962G>C	NP_059989.3:p.Arg1321Pro