Canonical Allele Identifier: CA366388928

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634423
• MyVariant Identifiers: chr6:g.157469911C>A (hg19) ; chr6:g.157148777C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148777C>A , CM000668.2:g.157148777C>A	GRCh38
NC_000006.11:g.157469911C>A , CM000668.1:g.157469911C>A	GRCh37
NC_000006.10:g.157511603C>A	NCBI36
NG_032093.1:g.375848C>A
NG_032093.2:g.375848C>A
NG_066624.1:g.377752C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2915C>A	ENSP00000055163.8:p.Ala972Asp
ENST00000414678.8:c.2825C>A	ENSP00000412835.3:p.Ala942Asp
ENST00000637015.2:c.2915C>A	ENSP00000489729.2:p.Ala972Asp
ENST00000319584.11:c.929C>A	ENSP00000313006.7:p.Ala310Asp
ENST00000346085.10:c.2954C>A	ENSP00000344546.5:p.Ala985Asp
ENST00000350026.10:c.2666C>A	ENSP00000055163.7:p.Ala889Asp
ENST00000414678.7:c.1073C>A	ENSP00000412835.2:p.Ala358Asp
ENST00000452544.2:n.816C>A
ENST00000635849.1:c.236C>A	ENSP00000490948.1:p.Ala79Asp
ENST00000636426.1:n.49C>A
ENST00000636930.2:c.2915C>A MANE Select	ENSP00000490491.2:p.Ala972Asp
ENST00000637015.1:c.154C>A
ENST00000637810.1:c.416C>A	ENSP00000489636.1:p.Ala139Asp
ENST00000637904.1:c.416C>A	ENSP00000490550.1:p.Ala139Asp
ENST00000647938.1:c.2705C>A	ENSP00000498155.1:p.Ala902Asp
ENST00000674190.1:n.1664C>A
ENST00000319584.10:c.932C>A	ENSP00000313006.6:p.Ala311Asp
ENST00000346085.9:c.2705C>A	ENSP00000344546.4:p.Ala902Asp
ENST00000350026.9:c.2666C>A	ENSP00000055163.7:p.Ala889Asp
ENST00000414678.6:c.1073C>A	ENSP00000412835.2:p.Ala358Asp
ENST00000452544.1:n.762C>A
NM_017519.2:c.2666C>A	NP_059989.2:p.Ala889Asp
NM_020732.3:c.2705C>A	NP_065783.3:p.Ala902Asp
XM_005267069.3:c.2666C>A	XP_005267126.2:p.Ala889Asp
XM_011535984.1:c.1616C>A	XP_011534286.1:p.Ala539Asp
XM_011535985.1:c.1436C>A	XP_011534287.1:p.Ala479Asp
XM_011535986.1:c.1196C>A	XP_011534288.1:p.Ala399Asp
XM_011535987.1:c.815C>A	XP_011534289.1:p.Ala272Asp
XM_011535988.1:c.-20+15570C>A	XP_011534290.1:n.-20+15570C>A
NM_001346813.1:c.2666C>A	NP_001333742.1:p.Ala889Asp
NM_001363725.1:c.416C>A	NP_001350654.1:p.Ala139Asp
XM_011535984.2:c.2747C>A	XP_011534286.2:p.Ala916Asp
XM_011535988.3:c.-20+15570C>A	XP_011534290.1:n.-20+15570C>A
XM_017011103.2:c.2747C>A	XP_016866592.1:p.Ala916Asp
XM_017011104.1:c.2747C>A	XP_016866593.1:p.Ala916Asp
XM_017011105.2:c.2747C>A	XP_016866594.1:p.Ala916Asp
XM_017011106.2:c.2747C>A	XP_016866595.1:p.Ala916Asp
XM_017011107.2:c.2567C>A	XP_016866596.1:p.Ala856Asp
XR_002956289.1:n.2830C>A
NM_001363725.2:c.416C>A	NP_001350654.1:p.Ala139Asp
NM_001371656.1:c.2954C>A	NP_001358585.1:p.Ala985Asp
NM_001374820.1:c.2954C>A	NP_001361749.1:p.Ala985Asp
NM_001374828.1:c.2915C>A MANE Select	NP_001361757.1:p.Ala972Asp
NM_017519.3:c.2915C>A	NP_059989.3:p.Ala972Asp