Canonical Allele Identifier: CA366242141

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522295A>T (hg19) ; chr6:g.157201161A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201161A>T , CM000668.2:g.157201161A>T	GRCh38
NC_000006.11:g.157522295A>T , CM000668.1:g.157522295A>T	GRCh37
NC_000006.10:g.157563987A>T	NCBI36
NG_032093.1:g.428232A>T
NG_032093.2:g.428232A>T
NG_066624.1:g.430136A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4777A>T	ENSP00000055163.8:p.Met1593Leu
ENST00000414678.8:c.4846A>T	ENSP00000412835.3:p.Met1616Leu
ENST00000637015.2:c.5065A>T	ENSP00000489729.2:p.Met1689Leu
ENST00000346085.10:c.4816A>T	ENSP00000344546.5:p.Met1606Leu
ENST00000350026.10:c.4528A>T	ENSP00000055163.7:p.Met1510Leu
ENST00000414678.7:c.3094A>T	ENSP00000412835.2:p.Met1032Leu
ENST00000635849.1:c.2257A>T	ENSP00000490948.1:p.Met753Leu
ENST00000635957.1:c.1888A>T	ENSP00000490385.1:p.Met630Leu
ENST00000636227.1:n.3399A>T
ENST00000636254.1:n.856A>T
ENST00000636930.2:c.4936A>T MANE Select	ENSP00000490491.2:p.Met1646Leu
ENST00000636940.1:n.2933A>T
ENST00000637015.1:c.2304A>T
ENST00000637568.1:c.2218A>T
ENST00000637741.1:n.1602A>T
ENST00000637810.1:c.2278A>T	ENSP00000489636.1:p.Met760Leu
ENST00000637904.1:c.2437A>T	ENSP00000490550.1:p.Met813Leu
ENST00000647938.1:c.4567A>T	ENSP00000498155.1:p.Met1523Leu
ENST00000346085.9:c.4567A>T	ENSP00000344546.4:p.Met1523Leu
ENST00000350026.9:c.4528A>T	ENSP00000055163.7:p.Met1510Leu
ENST00000414678.6:c.3094A>T	ENSP00000412835.2:p.Met1032Leu
NM_017519.2:c.4528A>T	NP_059989.2:p.Met1510Leu
NM_020732.3:c.4567A>T	NP_065783.3:p.Met1523Leu
XM_005267069.3:c.4687A>T	XP_005267126.2:p.Met1563Leu
XM_011535984.1:c.3766A>T	XP_011534286.1:p.Met1256Leu
XM_011535985.1:c.3586A>T	XP_011534287.1:p.Met1196Leu
XM_011535986.1:c.3346A>T	XP_011534288.1:p.Met1116Leu
XM_011535987.1:c.2965A>T	XP_011534289.1:p.Met989Leu
XM_011535988.1:c.1828A>T	XP_011534290.1:p.Met610Leu
NM_001346813.1:c.4687A>T	NP_001333742.1:p.Met1563Leu
NM_001363725.1:c.2437A>T	NP_001350654.1:p.Met813Leu
XM_011535984.2:c.4897A>T	XP_011534286.2:p.Met1633Leu
XM_011535988.3:c.1828A>T	XP_011534290.1:p.Met610Leu
XM_017011103.2:c.4798A>T	XP_016866592.1:p.Met1600Leu
XM_017011104.1:c.4768A>T	XP_016866593.1:p.Met1590Leu
XM_017011105.2:c.4738A>T	XP_016866594.1:p.Met1580Leu
XM_017011106.2:c.4609A>T	XP_016866595.1:p.Met1537Leu
XM_017011107.2:c.4588A>T	XP_016866596.1:p.Met1530Leu
XR_002956289.1:n.4883A>T
NM_001363725.2:c.2437A>T	NP_001350654.1:p.Met813Leu
NM_001371656.1:c.4816A>T	NP_001358585.1:p.Met1606Leu
NM_001374820.1:c.4816A>T	NP_001361749.1:p.Met1606Leu
NM_001374828.1:c.4936A>T MANE Select	NP_001361757.1:p.Met1646Leu
NM_017519.3:c.4777A>T	NP_059989.3:p.Met1593Leu