Canonical Allele Identifier: CA366235292

Gene: ARID1B

Linked Data

• dbSNP Id: rs1382136581
• MyVariant Identifiers: chr6:g.157511244G>C (hg19) ; chr6:g.157190110G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190110G>C , CM000668.2:g.157190110G>C	GRCh38
NC_000006.11:g.157511244G>C , CM000668.1:g.157511244G>C	GRCh37
NC_000006.10:g.157552936G>C	NCBI36
NG_032093.1:g.417181G>C
NG_032093.2:g.417181G>C
NG_066624.1:g.419085G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3972G>C	ENSP00000055163.8:p.Met1324Ile
ENST00000414678.8:c.4041G>C	ENSP00000412835.3:p.Met1347Ile
ENST00000637015.2:c.4260G>C	ENSP00000489729.2:p.Met1420Ile
ENST00000346085.10:c.4011G>C	ENSP00000344546.5:p.Met1337Ile
ENST00000350026.10:c.3723G>C	ENSP00000055163.7:p.Met1241Ile
ENST00000414678.7:c.2289G>C	ENSP00000412835.2:p.Met763Ile
ENST00000635849.1:c.1452G>C	ENSP00000490948.1:p.Met484Ile
ENST00000635957.1:c.1083G>C	ENSP00000490385.1:p.Met361Ile
ENST00000636930.2:c.4131G>C MANE Select	ENSP00000490491.2:p.Met1377Ile
ENST00000636940.1:n.2128G>C
ENST00000637015.1:c.1499G>C
ENST00000637568.1:c.1413G>C
ENST00000637741.1:n.797G>C
ENST00000637810.1:c.1473G>C	ENSP00000489636.1:p.Met491Ile
ENST00000637904.1:c.1632G>C	ENSP00000490550.1:p.Met544Ile
ENST00000647938.1:c.3762G>C	ENSP00000498155.1:p.Met1254Ile
ENST00000346085.9:c.3762G>C	ENSP00000344546.4:p.Met1254Ile
ENST00000350026.9:c.3723G>C	ENSP00000055163.7:p.Met1241Ile
ENST00000414678.6:c.2289G>C	ENSP00000412835.2:p.Met763Ile
NM_017519.2:c.3723G>C	NP_059989.2:p.Met1241Ile
NM_020732.3:c.3762G>C	NP_065783.3:p.Met1254Ile
XM_005267069.3:c.3882G>C	XP_005267126.2:p.Met1294Ile
XM_011535984.1:c.2961G>C	XP_011534286.1:p.Met987Ile
XM_011535985.1:c.2781G>C	XP_011534287.1:p.Met927Ile
XM_011535986.1:c.2541G>C	XP_011534288.1:p.Met847Ile
XM_011535987.1:c.2160G>C	XP_011534289.1:p.Met720Ile
XM_011535988.1:c.1023G>C	XP_011534290.1:p.Met341Ile
NM_001346813.1:c.3882G>C	NP_001333742.1:p.Met1294Ile
NM_001363725.1:c.1632G>C	NP_001350654.1:p.Met544Ile
XM_011535984.2:c.4092G>C	XP_011534286.2:p.Met1364Ile
XM_011535988.3:c.1023G>C	XP_011534290.1:p.Met341Ile
XM_017011103.2:c.3993G>C	XP_016866592.1:p.Met1331Ile
XM_017011104.1:c.3963G>C	XP_016866593.1:p.Met1321Ile
XM_017011105.2:c.3933G>C	XP_016866594.1:p.Met1311Ile
XM_017011106.2:c.3804G>C	XP_016866595.1:p.Met1268Ile
XM_017011107.2:c.3783G>C	XP_016866596.1:p.Met1261Ile
XR_002956289.1:n.4175G>C
NM_001363725.2:c.1632G>C	NP_001350654.1:p.Met544Ile
NM_001371656.1:c.4011G>C	NP_001358585.1:p.Met1337Ile
NM_001374820.1:c.4011G>C	NP_001361749.1:p.Met1337Ile
NM_001374828.1:c.4131G>C MANE Select	NP_001361757.1:p.Met1377Ile
NM_017519.3:c.3972G>C	NP_059989.3:p.Met1324Ile