Canonical Allele Identifier: CA366241822

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522206T>G (hg19) ; chr6:g.157201072T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201072T>G , CM000668.2:g.157201072T>G	GRCh38
NC_000006.11:g.157522206T>G , CM000668.1:g.157522206T>G	GRCh37
NC_000006.10:g.157563898T>G	NCBI36
NG_032093.1:g.428143T>G
NG_032093.2:g.428143T>G
NG_066624.1:g.430047T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4688T>G	ENSP00000055163.8:p.Met1563Arg
ENST00000414678.8:c.4757T>G	ENSP00000412835.3:p.Met1586Arg
ENST00000637015.2:c.4976T>G	ENSP00000489729.2:p.Met1659Arg
ENST00000346085.10:c.4727T>G	ENSP00000344546.5:p.Met1576Arg
ENST00000350026.10:c.4439T>G	ENSP00000055163.7:p.Met1480Arg
ENST00000414678.7:c.3005T>G	ENSP00000412835.2:p.Met1002Arg
ENST00000635849.1:c.2168T>G	ENSP00000490948.1:p.Met723Arg
ENST00000635957.1:c.1799T>G	ENSP00000490385.1:p.Met600Arg
ENST00000636227.1:n.3310T>G
ENST00000636254.1:n.767T>G
ENST00000636930.2:c.4847T>G MANE Select	ENSP00000490491.2:p.Met1616Arg
ENST00000636940.1:n.2844T>G
ENST00000637015.1:c.2215T>G
ENST00000637568.1:c.2129T>G
ENST00000637741.1:n.1513T>G
ENST00000637810.1:c.2189T>G	ENSP00000489636.1:p.Met730Arg
ENST00000637904.1:c.2348T>G	ENSP00000490550.1:p.Met783Arg
ENST00000647938.1:c.4478T>G	ENSP00000498155.1:p.Met1493Arg
ENST00000346085.9:c.4478T>G	ENSP00000344546.4:p.Met1493Arg
ENST00000350026.9:c.4439T>G	ENSP00000055163.7:p.Met1480Arg
ENST00000414678.6:c.3005T>G	ENSP00000412835.2:p.Met1002Arg
NM_017519.2:c.4439T>G	NP_059989.2:p.Met1480Arg
NM_020732.3:c.4478T>G	NP_065783.3:p.Met1493Arg
XM_005267069.3:c.4598T>G	XP_005267126.2:p.Met1533Arg
XM_011535984.1:c.3677T>G	XP_011534286.1:p.Met1226Arg
XM_011535985.1:c.3497T>G	XP_011534287.1:p.Met1166Arg
XM_011535986.1:c.3257T>G	XP_011534288.1:p.Met1086Arg
XM_011535987.1:c.2876T>G	XP_011534289.1:p.Met959Arg
XM_011535988.1:c.1739T>G	XP_011534290.1:p.Met580Arg
NM_001346813.1:c.4598T>G	NP_001333742.1:p.Met1533Arg
NM_001363725.1:c.2348T>G	NP_001350654.1:p.Met783Arg
XM_011535984.2:c.4808T>G	XP_011534286.2:p.Met1603Arg
XM_011535988.3:c.1739T>G	XP_011534290.1:p.Met580Arg
XM_017011103.2:c.4709T>G	XP_016866592.1:p.Met1570Arg
XM_017011104.1:c.4679T>G	XP_016866593.1:p.Met1560Arg
XM_017011105.2:c.4649T>G	XP_016866594.1:p.Met1550Arg
XM_017011106.2:c.4520T>G	XP_016866595.1:p.Met1507Arg
XM_017011107.2:c.4499T>G	XP_016866596.1:p.Met1500Arg
XR_002956289.1:n.4794T>G
NM_001363725.2:c.2348T>G	NP_001350654.1:p.Met783Arg
NM_001371656.1:c.4727T>G	NP_001358585.1:p.Met1576Arg
NM_001374820.1:c.4727T>G	NP_001361749.1:p.Met1576Arg
NM_001374828.1:c.4847T>G MANE Select	NP_001361757.1:p.Met1616Arg
NM_017519.3:c.4688T>G	NP_059989.3:p.Met1563Arg