Canonical Allele Identifier: CA366388934

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2697094
• ClinVar RCV Id: RCV003543797
• MyVariant Identifiers: chr6:g.157469914G>A (hg19) ; chr6:g.157148780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148780G>A , CM000668.2:g.157148780G>A	GRCh38
NC_000006.11:g.157469914G>A , CM000668.1:g.157469914G>A	GRCh37
NC_000006.10:g.157511606G>A	NCBI36
NG_032093.1:g.375851G>A
NG_032093.2:g.375851G>A
NG_066624.1:g.377755G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2918G>A	ENSP00000055163.8:p.Gly973Glu
ENST00000414678.8:c.2828G>A	ENSP00000412835.3:p.Gly943Glu
ENST00000637015.2:c.2918G>A	ENSP00000489729.2:p.Gly973Glu
ENST00000319584.11:c.932G>A	ENSP00000313006.7:p.Gly311Glu
ENST00000346085.10:c.2957G>A	ENSP00000344546.5:p.Gly986Glu
ENST00000350026.10:c.2669G>A	ENSP00000055163.7:p.Gly890Glu
ENST00000414678.7:c.1076G>A	ENSP00000412835.2:p.Gly359Glu
ENST00000452544.2:n.819G>A
ENST00000635849.1:c.239G>A	ENSP00000490948.1:p.Gly80Glu
ENST00000636426.1:n.52G>A
ENST00000636930.2:c.2918G>A MANE Select	ENSP00000490491.2:p.Gly973Glu
ENST00000637015.1:c.157G>A
ENST00000637810.1:c.419G>A	ENSP00000489636.1:p.Gly140Glu
ENST00000637904.1:c.419G>A	ENSP00000490550.1:p.Gly140Glu
ENST00000647938.1:c.2708G>A	ENSP00000498155.1:p.Gly903Glu
ENST00000674190.1:n.1667G>A
ENST00000319584.10:c.935G>A	ENSP00000313006.6:p.Gly312Glu
ENST00000346085.9:c.2708G>A	ENSP00000344546.4:p.Gly903Glu
ENST00000350026.9:c.2669G>A	ENSP00000055163.7:p.Gly890Glu
ENST00000414678.6:c.1076G>A	ENSP00000412835.2:p.Gly359Glu
ENST00000452544.1:n.765G>A
NM_017519.2:c.2669G>A	NP_059989.2:p.Gly890Glu
NM_020732.3:c.2708G>A	NP_065783.3:p.Gly903Glu
XM_005267069.3:c.2669G>A	XP_005267126.2:p.Gly890Glu
XM_011535984.1:c.1619G>A	XP_011534286.1:p.Gly540Glu
XM_011535985.1:c.1439G>A	XP_011534287.1:p.Gly480Glu
XM_011535986.1:c.1199G>A	XP_011534288.1:p.Gly400Glu
XM_011535987.1:c.818G>A	XP_011534289.1:p.Gly273Glu
XM_011535988.1:c.-20+15573G>A	XP_011534290.1:n.-20+15573G>A
NM_001346813.1:c.2669G>A	NP_001333742.1:p.Gly890Glu
NM_001363725.1:c.419G>A	NP_001350654.1:p.Gly140Glu
XM_011535984.2:c.2750G>A	XP_011534286.2:p.Gly917Glu
XM_011535988.3:c.-20+15573G>A	XP_011534290.1:n.-20+15573G>A
XM_017011103.2:c.2750G>A	XP_016866592.1:p.Gly917Glu
XM_017011104.1:c.2750G>A	XP_016866593.1:p.Gly917Glu
XM_017011105.2:c.2750G>A	XP_016866594.1:p.Gly917Glu
XM_017011106.2:c.2750G>A	XP_016866595.1:p.Gly917Glu
XM_017011107.2:c.2570G>A	XP_016866596.1:p.Gly857Glu
XR_002956289.1:n.2833G>A
NM_001363725.2:c.419G>A	NP_001350654.1:p.Gly140Glu
NM_001371656.1:c.2957G>A	NP_001358585.1:p.Gly986Glu
NM_001374820.1:c.2957G>A	NP_001361749.1:p.Gly986Glu
NM_001374828.1:c.2918G>A MANE Select	NP_001361757.1:p.Gly973Glu
NM_017519.3:c.2918G>A	NP_059989.3:p.Gly973Glu