Canonical Allele Identifier: CA366388895

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469893T>A (hg19) ; chr6:g.157148759T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148759T>A , CM000668.2:g.157148759T>A	GRCh38
NC_000006.11:g.157469893T>A , CM000668.1:g.157469893T>A	GRCh37
NC_000006.10:g.157511585T>A	NCBI36
NG_032093.1:g.375830T>A
NG_032093.2:g.375830T>A
NG_066624.1:g.377734T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2897T>A	ENSP00000055163.8:p.Leu966Gln
ENST00000414678.8:c.2807T>A	ENSP00000412835.3:p.Leu936Gln
ENST00000637015.2:c.2897T>A	ENSP00000489729.2:p.Leu966Gln
ENST00000319584.11:c.911T>A	ENSP00000313006.7:p.Leu304Gln
ENST00000346085.10:c.2936T>A	ENSP00000344546.5:p.Leu979Gln
ENST00000350026.10:c.2648T>A	ENSP00000055163.7:p.Leu883Gln
ENST00000414678.7:c.1055T>A	ENSP00000412835.2:p.Leu352Gln
ENST00000452544.2:n.798T>A
ENST00000635849.1:c.218T>A	ENSP00000490948.1:p.Leu73Gln
ENST00000636426.1:n.31T>A
ENST00000636930.2:c.2897T>A MANE Select	ENSP00000490491.2:p.Leu966Gln
ENST00000637015.1:c.136T>A
ENST00000637810.1:c.398T>A	ENSP00000489636.1:p.Leu133Gln
ENST00000637904.1:c.398T>A	ENSP00000490550.1:p.Leu133Gln
ENST00000647938.1:c.2687T>A	ENSP00000498155.1:p.Leu896Gln
ENST00000674190.1:n.1646T>A
ENST00000319584.10:c.914T>A	ENSP00000313006.6:p.Leu305Gln
ENST00000346085.9:c.2687T>A	ENSP00000344546.4:p.Leu896Gln
ENST00000350026.9:c.2648T>A	ENSP00000055163.7:p.Leu883Gln
ENST00000414678.6:c.1055T>A	ENSP00000412835.2:p.Leu352Gln
ENST00000452544.1:n.744T>A
NM_017519.2:c.2648T>A	NP_059989.2:p.Leu883Gln
NM_020732.3:c.2687T>A	NP_065783.3:p.Leu896Gln
XM_005267069.3:c.2648T>A	XP_005267126.2:p.Leu883Gln
XM_011535984.1:c.1598T>A	XP_011534286.1:p.Leu533Gln
XM_011535985.1:c.1418T>A	XP_011534287.1:p.Leu473Gln
XM_011535986.1:c.1178T>A	XP_011534288.1:p.Leu393Gln
XM_011535987.1:c.797T>A	XP_011534289.1:p.Leu266Gln
XM_011535988.1:c.-20+15552T>A	XP_011534290.1:n.-20+15552T>A
NM_001346813.1:c.2648T>A	NP_001333742.1:p.Leu883Gln
NM_001363725.1:c.398T>A	NP_001350654.1:p.Leu133Gln
XM_011535984.2:c.2729T>A	XP_011534286.2:p.Leu910Gln
XM_011535988.3:c.-20+15552T>A	XP_011534290.1:n.-20+15552T>A
XM_017011103.2:c.2729T>A	XP_016866592.1:p.Leu910Gln
XM_017011104.1:c.2729T>A	XP_016866593.1:p.Leu910Gln
XM_017011105.2:c.2729T>A	XP_016866594.1:p.Leu910Gln
XM_017011106.2:c.2729T>A	XP_016866595.1:p.Leu910Gln
XM_017011107.2:c.2549T>A	XP_016866596.1:p.Leu850Gln
XR_002956289.1:n.2812T>A
NM_001363725.2:c.398T>A	NP_001350654.1:p.Leu133Gln
NM_001371656.1:c.2936T>A	NP_001358585.1:p.Leu979Gln
NM_001374820.1:c.2936T>A	NP_001361749.1:p.Leu979Gln
NM_001374828.1:c.2897T>A MANE Select	NP_001361757.1:p.Leu966Gln
NM_017519.3:c.2897T>A	NP_059989.3:p.Leu966Gln