Canonical Allele Identifier: CA366389285

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470073C>A (hg19) ; chr6:g.157148939C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148939C>A , CM000668.2:g.157148939C>A	GRCh38
NC_000006.11:g.157470073C>A , CM000668.1:g.157470073C>A	GRCh37
NC_000006.10:g.157511765C>A	NCBI36
NG_032093.1:g.376010C>A
NG_032093.2:g.376010C>A
NG_066624.1:g.377914C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3077C>A	ENSP00000055163.8:p.Ser1026Ter
ENST00000414678.8:c.2987C>A	ENSP00000412835.3:p.Ser996Ter
ENST00000637015.2:c.3077C>A	ENSP00000489729.2:p.Ser1026Ter
ENST00000319584.11:c.1091C>A	ENSP00000313006.7:p.Ser364Ter
ENST00000346085.10:c.3116C>A	ENSP00000344546.5:p.Ser1039Ter
ENST00000350026.10:c.2828C>A	ENSP00000055163.7:p.Ser943Ter
ENST00000414678.7:c.1235C>A	ENSP00000412835.2:p.Ser412Ter
ENST00000452544.2:n.978C>A
ENST00000635849.1:c.398C>A	ENSP00000490948.1:p.Ser133Ter
ENST00000635957.1:c.32C>A	ENSP00000490385.1:p.Ser11Ter
ENST00000636426.1:n.211C>A
ENST00000636930.2:c.3077C>A MANE Select	ENSP00000490491.2:p.Ser1026Ter
ENST00000637015.1:c.316C>A
ENST00000637568.1:c.120C>A
ENST00000637810.1:c.578C>A	ENSP00000489636.1:p.Ser193Ter
ENST00000637904.1:c.578C>A	ENSP00000490550.1:p.Ser193Ter
ENST00000647938.1:c.2867C>A	ENSP00000498155.1:p.Ser956Ter
ENST00000674190.1:n.1826C>A
ENST00000319584.10:c.1094C>A	ENSP00000313006.6:p.Ser365Ter
ENST00000346085.9:c.2867C>A	ENSP00000344546.4:p.Ser956Ter
ENST00000350026.9:c.2828C>A	ENSP00000055163.7:p.Ser943Ter
ENST00000400790.3:c.29C>A	ENSP00000383596.3:p.Ser10Ter
ENST00000414678.6:c.1235C>A	ENSP00000412835.2:p.Ser412Ter
ENST00000452544.1:n.924C>A
ENST00000478761.3:c.150C>A
NM_017519.2:c.2828C>A	NP_059989.2:p.Ser943Ter
NM_020732.3:c.2867C>A	NP_065783.3:p.Ser956Ter
XM_005267069.3:c.2828C>A	XP_005267126.2:p.Ser943Ter
XM_011535984.1:c.1778C>A	XP_011534286.1:p.Ser593Ter
XM_011535985.1:c.1598C>A	XP_011534287.1:p.Ser533Ter
XM_011535986.1:c.1358C>A	XP_011534288.1:p.Ser453Ter
XM_011535987.1:c.977C>A	XP_011534289.1:p.Ser326Ter
XM_011535988.1:c.-20+15732C>A	XP_011534290.1:n.-20+15732C>A
NM_001346813.1:c.2828C>A	NP_001333742.1:p.Ser943Ter
NM_001363725.1:c.578C>A	NP_001350654.1:p.Ser193Ter
XM_011535984.2:c.2909C>A	XP_011534286.2:p.Ser970Ter
XM_011535988.3:c.-20+15732C>A	XP_011534290.1:n.-20+15732C>A
XM_017011103.2:c.2909C>A	XP_016866592.1:p.Ser970Ter
XM_017011104.1:c.2909C>A	XP_016866593.1:p.Ser970Ter
XM_017011105.2:c.2909C>A	XP_016866594.1:p.Ser970Ter
XM_017011106.2:c.2909C>A	XP_016866595.1:p.Ser970Ter
XM_017011107.2:c.2729C>A	XP_016866596.1:p.Ser910Ter
XR_002956289.1:n.2992C>A
NM_001363725.2:c.578C>A	NP_001350654.1:p.Ser193Ter
NM_001371656.1:c.3116C>A	NP_001358585.1:p.Ser1039Ter
NM_001374820.1:c.3116C>A	NP_001361749.1:p.Ser1039Ter
NM_001374828.1:c.3077C>A MANE Select	NP_001361757.1:p.Ser1026Ter
NM_017519.3:c.3077C>A	NP_059989.3:p.Ser1026Ter