Canonical Allele Identifier: CA366388647

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469781T>A (hg19) ; chr6:g.157148647T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148647T>A , CM000668.2:g.157148647T>A	GRCh38
NC_000006.11:g.157469781T>A , CM000668.1:g.157469781T>A	GRCh37
NC_000006.10:g.157511473T>A	NCBI36
NG_032093.1:g.375718T>A
NG_032093.2:g.375718T>A
NG_066624.1:g.377622T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2785T>A	ENSP00000055163.8:p.Tyr929Asn
ENST00000414678.8:c.2695T>A	ENSP00000412835.3:p.Tyr899Asn
ENST00000637015.2:c.2785T>A	ENSP00000489729.2:p.Tyr929Asn
ENST00000319584.11:c.799T>A	ENSP00000313006.7:p.Tyr267Asn
ENST00000346085.10:c.2824T>A	ENSP00000344546.5:p.Tyr942Asn
ENST00000350026.10:c.2536T>A	ENSP00000055163.7:p.Tyr846Asn
ENST00000414678.7:c.943T>A	ENSP00000412835.2:p.Tyr315Asn
ENST00000452544.2:n.686T>A
ENST00000635849.1:c.106T>A	ENSP00000490948.1:p.Tyr36Asn
ENST00000636930.2:c.2785T>A MANE Select	ENSP00000490491.2:p.Tyr929Asn
ENST00000637015.1:c.24T>A
ENST00000637810.1:c.286T>A	ENSP00000489636.1:p.Tyr96Asn
ENST00000637904.1:c.286T>A	ENSP00000490550.1:p.Tyr96Asn
ENST00000647938.1:c.2575T>A	ENSP00000498155.1:p.Tyr859Asn
ENST00000674190.1:n.1534T>A
ENST00000319584.10:c.802T>A	ENSP00000313006.6:p.Tyr268Asn
ENST00000346085.9:c.2575T>A	ENSP00000344546.4:p.Tyr859Asn
ENST00000350026.9:c.2536T>A	ENSP00000055163.7:p.Tyr846Asn
ENST00000414678.6:c.943T>A	ENSP00000412835.2:p.Tyr315Asn
ENST00000452544.1:n.632T>A
NM_017519.2:c.2536T>A	NP_059989.2:p.Tyr846Asn
NM_020732.3:c.2575T>A	NP_065783.3:p.Tyr859Asn
XM_005267069.3:c.2536T>A	XP_005267126.2:p.Tyr846Asn
XM_011535984.1:c.1486T>A	XP_011534286.1:p.Tyr496Asn
XM_011535985.1:c.1306T>A	XP_011534287.1:p.Tyr436Asn
XM_011535986.1:c.1066T>A	XP_011534288.1:p.Tyr356Asn
XM_011535987.1:c.685T>A	XP_011534289.1:p.Tyr229Asn
XM_011535988.1:c.-20+15440T>A	XP_011534290.1:n.-20+15440T>A
NM_001346813.1:c.2536T>A	NP_001333742.1:p.Tyr846Asn
NM_001363725.1:c.286T>A	NP_001350654.1:p.Tyr96Asn
XM_011535984.2:c.2617T>A	XP_011534286.2:p.Tyr873Asn
XM_011535988.3:c.-20+15440T>A	XP_011534290.1:n.-20+15440T>A
XM_017011103.2:c.2617T>A	XP_016866592.1:p.Tyr873Asn
XM_017011104.1:c.2617T>A	XP_016866593.1:p.Tyr873Asn
XM_017011105.2:c.2617T>A	XP_016866594.1:p.Tyr873Asn
XM_017011106.2:c.2617T>A	XP_016866595.1:p.Tyr873Asn
XM_017011107.2:c.2437T>A	XP_016866596.1:p.Tyr813Asn
XR_002956289.1:n.2700T>A
NM_001363725.2:c.286T>A	NP_001350654.1:p.Tyr96Asn
NM_001371656.1:c.2824T>A	NP_001358585.1:p.Tyr942Asn
NM_001374820.1:c.2824T>A	NP_001361749.1:p.Tyr942Asn
NM_001374828.1:c.2785T>A MANE Select	NP_001361757.1:p.Tyr929Asn
NM_017519.3:c.2785T>A	NP_059989.3:p.Tyr929Asn