Canonical Allele Identifier: CA366389179

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470024C>A (hg19) ; chr6:g.157148890C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148890C>A , CM000668.2:g.157148890C>A	GRCh38
NC_000006.11:g.157470024C>A , CM000668.1:g.157470024C>A	GRCh37
NC_000006.10:g.157511716C>A	NCBI36
NG_032093.1:g.375961C>A
NG_032093.2:g.375961C>A
NG_066624.1:g.377865C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3028C>A	ENSP00000055163.8:p.Arg1010Ser
ENST00000414678.8:c.2938C>A	ENSP00000412835.3:p.Arg980Ser
ENST00000637015.2:c.3028C>A	ENSP00000489729.2:p.Arg1010Ser
ENST00000319584.11:c.1042C>A	ENSP00000313006.7:p.Arg348Ser
ENST00000346085.10:c.3067C>A	ENSP00000344546.5:p.Arg1023Ser
ENST00000350026.10:c.2779C>A	ENSP00000055163.7:p.Arg927Ser
ENST00000414678.7:c.1186C>A	ENSP00000412835.2:p.Arg396Ser
ENST00000452544.2:n.929C>A
ENST00000635849.1:c.349C>A	ENSP00000490948.1:p.Arg117Ser
ENST00000636426.1:n.162C>A
ENST00000636930.2:c.3028C>A MANE Select	ENSP00000490491.2:p.Arg1010Ser
ENST00000637015.1:c.267C>A
ENST00000637568.1:c.71C>A
ENST00000637810.1:c.529C>A	ENSP00000489636.1:p.Arg177Ser
ENST00000637904.1:c.529C>A	ENSP00000490550.1:p.Arg177Ser
ENST00000647938.1:c.2818C>A	ENSP00000498155.1:p.Arg940Ser
ENST00000674190.1:n.1777C>A
ENST00000319584.10:c.1045C>A	ENSP00000313006.6:p.Arg349Ser
ENST00000346085.9:c.2818C>A	ENSP00000344546.4:p.Arg940Ser
ENST00000350026.9:c.2779C>A	ENSP00000055163.7:p.Arg927Ser
ENST00000414678.6:c.1186C>A	ENSP00000412835.2:p.Arg396Ser
ENST00000452544.1:n.875C>A
ENST00000478761.3:c.101C>A
NM_017519.2:c.2779C>A	NP_059989.2:p.Arg927Ser
NM_020732.3:c.2818C>A	NP_065783.3:p.Arg940Ser
XM_005267069.3:c.2779C>A	XP_005267126.2:p.Arg927Ser
XM_011535984.1:c.1729C>A	XP_011534286.1:p.Arg577Ser
XM_011535985.1:c.1549C>A	XP_011534287.1:p.Arg517Ser
XM_011535986.1:c.1309C>A	XP_011534288.1:p.Arg437Ser
XM_011535987.1:c.928C>A	XP_011534289.1:p.Arg310Ser
XM_011535988.1:c.-20+15683C>A	XP_011534290.1:n.-20+15683C>A
NM_001346813.1:c.2779C>A	NP_001333742.1:p.Arg927Ser
NM_001363725.1:c.529C>A	NP_001350654.1:p.Arg177Ser
XM_011535984.2:c.2860C>A	XP_011534286.2:p.Arg954Ser
XM_011535988.3:c.-20+15683C>A	XP_011534290.1:n.-20+15683C>A
XM_017011103.2:c.2860C>A	XP_016866592.1:p.Arg954Ser
XM_017011104.1:c.2860C>A	XP_016866593.1:p.Arg954Ser
XM_017011105.2:c.2860C>A	XP_016866594.1:p.Arg954Ser
XM_017011106.2:c.2860C>A	XP_016866595.1:p.Arg954Ser
XM_017011107.2:c.2680C>A	XP_016866596.1:p.Arg894Ser
XR_002956289.1:n.2943C>A
NM_001363725.2:c.529C>A	NP_001350654.1:p.Arg177Ser
NM_001371656.1:c.3067C>A	NP_001358585.1:p.Arg1023Ser
NM_001374820.1:c.3067C>A	NP_001361749.1:p.Arg1023Ser
NM_001374828.1:c.3028C>A MANE Select	NP_001361757.1:p.Arg1010Ser
NM_017519.3:c.3028C>A	NP_059989.3:p.Arg1010Ser