Canonical Allele Identifier: CA366241367

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522118A>T (hg19) ; chr6:g.157200984A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200984A>T , CM000668.2:g.157200984A>T	GRCh38
NC_000006.11:g.157522118A>T , CM000668.1:g.157522118A>T	GRCh37
NC_000006.10:g.157563810A>T	NCBI36
NG_032093.1:g.428055A>T
NG_032093.2:g.428055A>T
NG_066624.1:g.429959A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4600A>T	ENSP00000055163.8:p.Met1534Leu
ENST00000414678.8:c.4669A>T	ENSP00000412835.3:p.Met1557Leu
ENST00000637015.2:c.4888A>T	ENSP00000489729.2:p.Met1630Leu
ENST00000346085.10:c.4639A>T	ENSP00000344546.5:p.Met1547Leu
ENST00000350026.10:c.4351A>T	ENSP00000055163.7:p.Met1451Leu
ENST00000414678.7:c.2917A>T	ENSP00000412835.2:p.Met973Leu
ENST00000635849.1:c.2080A>T	ENSP00000490948.1:p.Met694Leu
ENST00000635957.1:c.1711A>T	ENSP00000490385.1:p.Met571Leu
ENST00000636227.1:n.3222A>T
ENST00000636254.1:n.679A>T
ENST00000636930.2:c.4759A>T MANE Select	ENSP00000490491.2:p.Met1587Leu
ENST00000636940.1:n.2756A>T
ENST00000637015.1:c.2127A>T
ENST00000637568.1:c.2041A>T
ENST00000637741.1:n.1425A>T
ENST00000637810.1:c.2101A>T	ENSP00000489636.1:p.Met701Leu
ENST00000637904.1:c.2260A>T	ENSP00000490550.1:p.Met754Leu
ENST00000647938.1:c.4390A>T	ENSP00000498155.1:p.Met1464Leu
ENST00000346085.9:c.4390A>T	ENSP00000344546.4:p.Met1464Leu
ENST00000350026.9:c.4351A>T	ENSP00000055163.7:p.Met1451Leu
ENST00000414678.6:c.2917A>T	ENSP00000412835.2:p.Met973Leu
NM_017519.2:c.4351A>T	NP_059989.2:p.Met1451Leu
NM_020732.3:c.4390A>T	NP_065783.3:p.Met1464Leu
XM_005267069.3:c.4510A>T	XP_005267126.2:p.Met1504Leu
XM_011535984.1:c.3589A>T	XP_011534286.1:p.Met1197Leu
XM_011535985.1:c.3409A>T	XP_011534287.1:p.Met1137Leu
XM_011535986.1:c.3169A>T	XP_011534288.1:p.Met1057Leu
XM_011535987.1:c.2788A>T	XP_011534289.1:p.Met930Leu
XM_011535988.1:c.1651A>T	XP_011534290.1:p.Met551Leu
NM_001346813.1:c.4510A>T	NP_001333742.1:p.Met1504Leu
NM_001363725.1:c.2260A>T	NP_001350654.1:p.Met754Leu
XM_011535984.2:c.4720A>T	XP_011534286.2:p.Met1574Leu
XM_011535988.3:c.1651A>T	XP_011534290.1:p.Met551Leu
XM_017011103.2:c.4621A>T	XP_016866592.1:p.Met1541Leu
XM_017011104.1:c.4591A>T	XP_016866593.1:p.Met1531Leu
XM_017011105.2:c.4561A>T	XP_016866594.1:p.Met1521Leu
XM_017011106.2:c.4432A>T	XP_016866595.1:p.Met1478Leu
XM_017011107.2:c.4411A>T	XP_016866596.1:p.Met1471Leu
XR_002956289.1:n.4706A>T
NM_001363725.2:c.2260A>T	NP_001350654.1:p.Met754Leu
NM_001371656.1:c.4639A>T	NP_001358585.1:p.Met1547Leu
NM_001374820.1:c.4639A>T	NP_001361749.1:p.Met1547Leu
NM_001374828.1:c.4759A>T MANE Select	NP_001361757.1:p.Met1587Leu
NM_017519.3:c.4600A>T	NP_059989.3:p.Met1534Leu