Canonical Allele Identifier: CA1675517029

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148808T= , CM000668.2:g.157148808T=	GRCh38
NC_000006.11:g.157469942T= , CM000668.1:g.157469942T=	GRCh37
NC_000006.10:g.157511634T=	NCBI36
NG_032093.1:g.375879T=
NG_032093.2:g.375879T=
NG_066624.1:g.377783T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2946T=	ENSP00000055163.8:p.Asn982=
ENST00000414678.8:c.2856T=	ENSP00000412835.3:p.Asn952=
ENST00000637015.2:c.2946T=	ENSP00000489729.2:p.Asn982=
ENST00000319584.11:c.960T=	ENSP00000313006.7:p.Asn320=
ENST00000346085.10:c.2985T=	ENSP00000344546.5:p.Asn995=
ENST00000350026.10:c.2697T=	ENSP00000055163.7:p.Asn899=
ENST00000414678.7:c.1104T=	ENSP00000412835.2:p.Asn368=
ENST00000452544.2:n.847T=
ENST00000635849.1:c.267T=	ENSP00000490948.1:p.Asn89=
ENST00000636426.1:n.80T=
ENST00000636930.2:c.2946T= MANE Select	ENSP00000490491.2:p.Asn982=
ENST00000637015.1:c.185T=
ENST00000637810.1:c.447T=	ENSP00000489636.1:p.Asn149=
ENST00000637904.1:c.447T=	ENSP00000490550.1:p.Asn149=
ENST00000647938.1:c.2736T=	ENSP00000498155.1:p.Asn912=
ENST00000674190.1:n.1695T=
ENST00000319584.10:c.963T=	ENSP00000313006.6:p.Asn321=
ENST00000346085.9:c.2736T=	ENSP00000344546.4:p.Asn912=
ENST00000350026.9:c.2697T=	ENSP00000055163.7:p.Asn899=
ENST00000414678.6:c.1104T=	ENSP00000412835.2:p.Asn368=
ENST00000452544.1:n.793T=
ENST00000478761.3:c.19T=
NM_017519.2:c.2697T=	NP_059989.2:p.Asn899=
NM_020732.3:c.2736T=	NP_065783.3:p.Asn912=
XM_005267069.3:c.2697T=	XP_005267126.2:p.Asn899=
XM_011535984.1:c.1647T=	XP_011534286.1:p.Asn549=
XM_011535985.1:c.1467T=	XP_011534287.1:p.Asn489=
XM_011535986.1:c.1227T=	XP_011534288.1:p.Asn409=
XM_011535987.1:c.846T=	XP_011534289.1:p.Asn282=
XM_011535988.1:c.-20+15601T=	XP_011534290.1:n.-20+15601T=
NM_001346813.1:c.2697T=	NP_001333742.1:p.Asn899=
NM_001363725.1:c.447T=	NP_001350654.1:p.Asn149=
XM_011535984.2:c.2778T=	XP_011534286.2:p.Asn926=
XM_011535988.3:c.-20+15601T=	XP_011534290.1:n.-20+15601T=
XM_017011103.2:c.2778T=	XP_016866592.1:p.Asn926=
XM_017011104.1:c.2778T=	XP_016866593.1:p.Asn926=
XM_017011105.2:c.2778T=	XP_016866594.1:p.Asn926=
XM_017011106.2:c.2778T=	XP_016866595.1:p.Asn926=
XM_017011107.2:c.2598T=	XP_016866596.1:p.Asn866=
XR_002956289.1:n.2861T=
NM_001363725.2:c.447T=	NP_001350654.1:p.Asn149=
NM_001371656.1:c.2985T=	NP_001358585.1:p.Asn995=
NM_001374820.1:c.2985T=	NP_001361749.1:p.Asn995=
NM_001374828.1:c.2946T= MANE Select	NP_001361757.1:p.Asn982=
NM_017519.3:c.2946T=	NP_059989.3:p.Asn982=