Canonical Allele Identifier: CA366388922

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148774C>A , CM000668.2:g.157148774C>A	GRCh38
NC_000006.11:g.157469908C>A , CM000668.1:g.157469908C>A	GRCh37
NC_000006.10:g.157511600C>A	NCBI36
NG_032093.1:g.375845C>A
NG_032093.2:g.375845C>A
NG_066624.1:g.377749C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2912C>A	ENSP00000055163.8:p.Ser971Ter
ENST00000414678.8:c.2822C>A	ENSP00000412835.3:p.Ser941Ter
ENST00000637015.2:c.2912C>A	ENSP00000489729.2:p.Ser971Ter
ENST00000319584.11:c.926C>A	ENSP00000313006.7:p.Ser309Ter
ENST00000346085.10:c.2951C>A	ENSP00000344546.5:p.Ser984Ter
ENST00000350026.10:c.2663C>A	ENSP00000055163.7:p.Ser888Ter
ENST00000414678.7:c.1070C>A	ENSP00000412835.2:p.Ser357Ter
ENST00000452544.2:n.813C>A
ENST00000635849.1:c.233C>A	ENSP00000490948.1:p.Ser78Ter
ENST00000636426.1:n.46C>A
ENST00000636930.2:c.2912C>A MANE Select	ENSP00000490491.2:p.Ser971Ter
ENST00000637015.1:c.151C>A
ENST00000637810.1:c.413C>A	ENSP00000489636.1:p.Ser138Ter
ENST00000637904.1:c.413C>A	ENSP00000490550.1:p.Ser138Ter
ENST00000647938.1:c.2702C>A	ENSP00000498155.1:p.Ser901Ter
ENST00000674190.1:n.1661C>A
ENST00000319584.10:c.929C>A	ENSP00000313006.6:p.Ser310Ter
ENST00000346085.9:c.2702C>A	ENSP00000344546.4:p.Ser901Ter
ENST00000350026.9:c.2663C>A	ENSP00000055163.7:p.Ser888Ter
ENST00000414678.6:c.1070C>A	ENSP00000412835.2:p.Ser357Ter
ENST00000452544.1:n.759C>A
NM_017519.2:c.2663C>A	NP_059989.2:p.Ser888Ter
NM_020732.3:c.2702C>A	NP_065783.3:p.Ser901Ter
XM_005267069.3:c.2663C>A	XP_005267126.2:p.Ser888Ter
XM_011535984.1:c.1613C>A	XP_011534286.1:p.Ser538Ter
XM_011535985.1:c.1433C>A	XP_011534287.1:p.Ser478Ter
XM_011535986.1:c.1193C>A	XP_011534288.1:p.Ser398Ter
XM_011535987.1:c.812C>A	XP_011534289.1:p.Ser271Ter
XM_011535988.1:c.-20+15567C>A	XP_011534290.1:n.-20+15567C>A
NM_001346813.1:c.2663C>A	NP_001333742.1:p.Ser888Ter
NM_001363725.1:c.413C>A	NP_001350654.1:p.Ser138Ter
XM_011535984.2:c.2744C>A	XP_011534286.2:p.Ser915Ter
XM_011535988.3:c.-20+15567C>A	XP_011534290.1:n.-20+15567C>A
XM_017011103.2:c.2744C>A	XP_016866592.1:p.Ser915Ter
XM_017011104.1:c.2744C>A	XP_016866593.1:p.Ser915Ter
XM_017011105.2:c.2744C>A	XP_016866594.1:p.Ser915Ter
XM_017011106.2:c.2744C>A	XP_016866595.1:p.Ser915Ter
XM_017011107.2:c.2564C>A	XP_016866596.1:p.Ser855Ter
XR_002956289.1:n.2827C>A
NM_001363725.2:c.413C>A	NP_001350654.1:p.Ser138Ter
NM_001371656.1:c.2951C>A	NP_001358585.1:p.Ser984Ter
NM_001374820.1:c.2951C>A	NP_001361749.1:p.Ser984Ter
NM_001374828.1:c.2912C>A MANE Select	NP_001361757.1:p.Ser971Ter
NM_017519.3:c.2912C>A	NP_059989.3:p.Ser971Ter