Canonical Allele Identifier: CA452978315

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522129A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200995A>T , CM000668.2:g.157200995A>T	GRCh38
NC_000006.11:g.157522129A>T , CM000668.1:g.157522129A>T	GRCh37
NC_000006.10:g.157563821A>T	NCBI36
NG_032093.1:g.428066A>T
NG_032093.2:g.428066A>T
NG_066624.1:g.429970A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4611A>T	ENSP00000055163.8:p.Ala1537=
ENST00000414678.8:c.4680A>T	ENSP00000412835.3:p.Ala1560=
ENST00000637015.2:c.4899A>T	ENSP00000489729.2:p.Ala1633=
ENST00000346085.10:c.4650A>T	ENSP00000344546.5:p.Ala1550=
ENST00000350026.10:c.4362A>T	ENSP00000055163.7:p.Ala1454=
ENST00000414678.7:c.2928A>T	ENSP00000412835.2:p.Ala976=
ENST00000635849.1:c.2091A>T	ENSP00000490948.1:p.Ala697=
ENST00000635957.1:c.1722A>T	ENSP00000490385.1:p.Ala574=
ENST00000636227.1:n.3233A>T
ENST00000636254.1:n.690A>T
ENST00000636930.2:c.4770A>T MANE Select	ENSP00000490491.2:p.Ala1590=
ENST00000636940.1:n.2767A>T
ENST00000637015.1:c.2138A>T
ENST00000637568.1:c.2052A>T
ENST00000637741.1:n.1436A>T
ENST00000637810.1:c.2112A>T	ENSP00000489636.1:p.Ala704=
ENST00000637904.1:c.2271A>T	ENSP00000490550.1:p.Ala757=
ENST00000647938.1:c.4401A>T	ENSP00000498155.1:p.Ala1467=
ENST00000346085.9:c.4401A>T	ENSP00000344546.4:p.Ala1467=
ENST00000350026.9:c.4362A>T	ENSP00000055163.7:p.Ala1454=
ENST00000414678.6:c.2928A>T	ENSP00000412835.2:p.Ala976=
NM_017519.2:c.4362A>T	NP_059989.2:p.Ala1454=
NM_020732.3:c.4401A>T	NP_065783.3:p.Ala1467=
XM_005267069.3:c.4521A>T	XP_005267126.2:p.Ala1507=
XM_011535984.1:c.3600A>T	XP_011534286.1:p.Ala1200=
XM_011535985.1:c.3420A>T	XP_011534287.1:p.Ala1140=
XM_011535986.1:c.3180A>T	XP_011534288.1:p.Ala1060=
XM_011535987.1:c.2799A>T	XP_011534289.1:p.Ala933=
XM_011535988.1:c.1662A>T	XP_011534290.1:p.Ala554=
NM_001346813.1:c.4521A>T	NP_001333742.1:p.Ala1507=
NM_001363725.1:c.2271A>T	NP_001350654.1:p.Ala757=
XM_011535984.2:c.4731A>T	XP_011534286.2:p.Ala1577=
XM_011535988.3:c.1662A>T	XP_011534290.1:p.Ala554=
XM_017011103.2:c.4632A>T	XP_016866592.1:p.Ala1544=
XM_017011104.1:c.4602A>T	XP_016866593.1:p.Ala1534=
XM_017011105.2:c.4572A>T	XP_016866594.1:p.Ala1524=
XM_017011106.2:c.4443A>T	XP_016866595.1:p.Ala1481=
XM_017011107.2:c.4422A>T	XP_016866596.1:p.Ala1474=
XR_002956289.1:n.4717A>T
NM_001363725.2:c.2271A>T	NP_001350654.1:p.Ala757=
NM_001371656.1:c.4650A>T	NP_001358585.1:p.Ala1550=
NM_001374820.1:c.4650A>T	NP_001361749.1:p.Ala1550=
NM_001374828.1:c.4770A>T MANE Select	NP_001361757.1:p.Ala1590=
NM_017519.3:c.4611A>T	NP_059989.3:p.Ala1537=