Canonical Allele Identifier: CA366388925

Gene: ARID1B

Linked Data

• dbSNP Id: rs1583405232
• gnomAD v4: 6-157148776-G-A
• MyVariant Identifiers: chr6:g.157469910G>A (hg19) ; chr6:g.157148776G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148776G>A , CM000668.2:g.157148776G>A	GRCh38
NC_000006.11:g.157469910G>A , CM000668.1:g.157469910G>A	GRCh37
NC_000006.10:g.157511602G>A	NCBI36
NG_032093.1:g.375847G>A
NG_032093.2:g.375847G>A
NG_066624.1:g.377751G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2914G>A	ENSP00000055163.8:p.Ala972Thr
ENST00000414678.8:c.2824G>A	ENSP00000412835.3:p.Ala942Thr
ENST00000637015.2:c.2914G>A	ENSP00000489729.2:p.Ala972Thr
ENST00000319584.11:c.928G>A	ENSP00000313006.7:p.Ala310Thr
ENST00000346085.10:c.2953G>A	ENSP00000344546.5:p.Ala985Thr
ENST00000350026.10:c.2665G>A	ENSP00000055163.7:p.Ala889Thr
ENST00000414678.7:c.1072G>A	ENSP00000412835.2:p.Ala358Thr
ENST00000452544.2:n.815G>A
ENST00000635849.1:c.235G>A	ENSP00000490948.1:p.Ala79Thr
ENST00000636426.1:n.48G>A
ENST00000636930.2:c.2914G>A MANE Select	ENSP00000490491.2:p.Ala972Thr
ENST00000637015.1:c.153G>A
ENST00000637810.1:c.415G>A	ENSP00000489636.1:p.Ala139Thr
ENST00000637904.1:c.415G>A	ENSP00000490550.1:p.Ala139Thr
ENST00000647938.1:c.2704G>A	ENSP00000498155.1:p.Ala902Thr
ENST00000674190.1:n.1663G>A
ENST00000319584.10:c.931G>A	ENSP00000313006.6:p.Ala311Thr
ENST00000346085.9:c.2704G>A	ENSP00000344546.4:p.Ala902Thr
ENST00000350026.9:c.2665G>A	ENSP00000055163.7:p.Ala889Thr
ENST00000414678.6:c.1072G>A	ENSP00000412835.2:p.Ala358Thr
ENST00000452544.1:n.761G>A
NM_017519.2:c.2665G>A	NP_059989.2:p.Ala889Thr
NM_020732.3:c.2704G>A	NP_065783.3:p.Ala902Thr
XM_005267069.3:c.2665G>A	XP_005267126.2:p.Ala889Thr
XM_011535984.1:c.1615G>A	XP_011534286.1:p.Ala539Thr
XM_011535985.1:c.1435G>A	XP_011534287.1:p.Ala479Thr
XM_011535986.1:c.1195G>A	XP_011534288.1:p.Ala399Thr
XM_011535987.1:c.814G>A	XP_011534289.1:p.Ala272Thr
XM_011535988.1:c.-20+15569G>A	XP_011534290.1:n.-20+15569G>A
NM_001346813.1:c.2665G>A	NP_001333742.1:p.Ala889Thr
NM_001363725.1:c.415G>A	NP_001350654.1:p.Ala139Thr
XM_011535984.2:c.2746G>A	XP_011534286.2:p.Ala916Thr
XM_011535988.3:c.-20+15569G>A	XP_011534290.1:n.-20+15569G>A
XM_017011103.2:c.2746G>A	XP_016866592.1:p.Ala916Thr
XM_017011104.1:c.2746G>A	XP_016866593.1:p.Ala916Thr
XM_017011105.2:c.2746G>A	XP_016866594.1:p.Ala916Thr
XM_017011106.2:c.2746G>A	XP_016866595.1:p.Ala916Thr
XM_017011107.2:c.2566G>A	XP_016866596.1:p.Ala856Thr
XR_002956289.1:n.2829G>A
NM_001363725.2:c.415G>A	NP_001350654.1:p.Ala139Thr
NM_001371656.1:c.2953G>A	NP_001358585.1:p.Ala985Thr
NM_001374820.1:c.2953G>A	NP_001361749.1:p.Ala985Thr
NM_001374828.1:c.2914G>A MANE Select	NP_001361757.1:p.Ala972Thr
NM_017519.3:c.2914G>A	NP_059989.3:p.Ala972Thr