Canonical Allele Identifier: CA366388971

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469929C>G (hg19) ; chr6:g.157148795C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148795C>G , CM000668.2:g.157148795C>G	GRCh38
NC_000006.11:g.157469929C>G , CM000668.1:g.157469929C>G	GRCh37
NC_000006.10:g.157511621C>G	NCBI36
NG_032093.1:g.375866C>G
NG_032093.2:g.375866C>G
NG_066624.1:g.377770C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2933C>G	ENSP00000055163.8:p.Pro978Arg
ENST00000414678.8:c.2843C>G	ENSP00000412835.3:p.Pro948Arg
ENST00000637015.2:c.2933C>G	ENSP00000489729.2:p.Pro978Arg
ENST00000319584.11:c.947C>G	ENSP00000313006.7:p.Pro316Arg
ENST00000346085.10:c.2972C>G	ENSP00000344546.5:p.Pro991Arg
ENST00000350026.10:c.2684C>G	ENSP00000055163.7:p.Pro895Arg
ENST00000414678.7:c.1091C>G	ENSP00000412835.2:p.Pro364Arg
ENST00000452544.2:n.834C>G
ENST00000635849.1:c.254C>G	ENSP00000490948.1:p.Pro85Arg
ENST00000636426.1:n.67C>G
ENST00000636930.2:c.2933C>G MANE Select	ENSP00000490491.2:p.Pro978Arg
ENST00000637015.1:c.172C>G
ENST00000637810.1:c.434C>G	ENSP00000489636.1:p.Pro145Arg
ENST00000637904.1:c.434C>G	ENSP00000490550.1:p.Pro145Arg
ENST00000647938.1:c.2723C>G	ENSP00000498155.1:p.Pro908Arg
ENST00000674190.1:n.1682C>G
ENST00000319584.10:c.950C>G	ENSP00000313006.6:p.Pro317Arg
ENST00000346085.9:c.2723C>G	ENSP00000344546.4:p.Pro908Arg
ENST00000350026.9:c.2684C>G	ENSP00000055163.7:p.Pro895Arg
ENST00000414678.6:c.1091C>G	ENSP00000412835.2:p.Pro364Arg
ENST00000452544.1:n.780C>G
ENST00000478761.3:c.6C>G
NM_017519.2:c.2684C>G	NP_059989.2:p.Pro895Arg
NM_020732.3:c.2723C>G	NP_065783.3:p.Pro908Arg
XM_005267069.3:c.2684C>G	XP_005267126.2:p.Pro895Arg
XM_011535984.1:c.1634C>G	XP_011534286.1:p.Pro545Arg
XM_011535985.1:c.1454C>G	XP_011534287.1:p.Pro485Arg
XM_011535986.1:c.1214C>G	XP_011534288.1:p.Pro405Arg
XM_011535987.1:c.833C>G	XP_011534289.1:p.Pro278Arg
XM_011535988.1:c.-20+15588C>G	XP_011534290.1:n.-20+15588C>G
NM_001346813.1:c.2684C>G	NP_001333742.1:p.Pro895Arg
NM_001363725.1:c.434C>G	NP_001350654.1:p.Pro145Arg
XM_011535984.2:c.2765C>G	XP_011534286.2:p.Pro922Arg
XM_011535988.3:c.-20+15588C>G	XP_011534290.1:n.-20+15588C>G
XM_017011103.2:c.2765C>G	XP_016866592.1:p.Pro922Arg
XM_017011104.1:c.2765C>G	XP_016866593.1:p.Pro922Arg
XM_017011105.2:c.2765C>G	XP_016866594.1:p.Pro922Arg
XM_017011106.2:c.2765C>G	XP_016866595.1:p.Pro922Arg
XM_017011107.2:c.2585C>G	XP_016866596.1:p.Pro862Arg
XR_002956289.1:n.2848C>G
NM_001363725.2:c.434C>G	NP_001350654.1:p.Pro145Arg
NM_001371656.1:c.2972C>G	NP_001358585.1:p.Pro991Arg
NM_001374820.1:c.2972C>G	NP_001361749.1:p.Pro991Arg
NM_001374828.1:c.2933C>G MANE Select	NP_001361757.1:p.Pro978Arg
NM_017519.3:c.2933C>G	NP_059989.3:p.Pro978Arg