Canonical Allele Identifier: CA1675517038

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148841G= , CM000668.2:g.157148841G=	GRCh38
NC_000006.11:g.157469975G= , CM000668.1:g.157469975G=	GRCh37
NC_000006.10:g.157511667G=	NCBI36
NG_032093.1:g.375912G=
NG_032093.2:g.375912G=
NG_066624.1:g.377816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2979G=	ENSP00000055163.8:p.Met993=
ENST00000414678.8:c.2889G=	ENSP00000412835.3:p.Met963=
ENST00000637015.2:c.2979G=	ENSP00000489729.2:p.Met993=
ENST00000319584.11:c.993G=	ENSP00000313006.7:p.Met331=
ENST00000346085.10:c.3018G=	ENSP00000344546.5:p.Met1006=
ENST00000350026.10:c.2730G=	ENSP00000055163.7:p.Met910=
ENST00000414678.7:c.1137G=	ENSP00000412835.2:p.Met379=
ENST00000452544.2:n.880G=
ENST00000635849.1:c.300G=	ENSP00000490948.1:p.Met100=
ENST00000636426.1:n.113G=
ENST00000636930.2:c.2979G= MANE Select	ENSP00000490491.2:p.Met993=
ENST00000637015.1:c.218G=
ENST00000637568.1:c.22G=
ENST00000637810.1:c.480G=	ENSP00000489636.1:p.Met160=
ENST00000637904.1:c.480G=	ENSP00000490550.1:p.Met160=
ENST00000647938.1:c.2769G=	ENSP00000498155.1:p.Met923=
ENST00000674190.1:n.1728G=
ENST00000319584.10:c.996G=	ENSP00000313006.6:p.Met332=
ENST00000346085.9:c.2769G=	ENSP00000344546.4:p.Met923=
ENST00000350026.9:c.2730G=	ENSP00000055163.7:p.Met910=
ENST00000414678.6:c.1137G=	ENSP00000412835.2:p.Met379=
ENST00000452544.1:n.826G=
ENST00000478761.3:c.52G=
NM_017519.2:c.2730G=	NP_059989.2:p.Met910=
NM_020732.3:c.2769G=	NP_065783.3:p.Met923=
XM_005267069.3:c.2730G=	XP_005267126.2:p.Met910=
XM_011535984.1:c.1680G=	XP_011534286.1:p.Met560=
XM_011535985.1:c.1500G=	XP_011534287.1:p.Met500=
XM_011535986.1:c.1260G=	XP_011534288.1:p.Met420=
XM_011535987.1:c.879G=	XP_011534289.1:p.Met293=
XM_011535988.1:c.-20+15634G=	XP_011534290.1:n.-20+15634G=
NM_001346813.1:c.2730G=	NP_001333742.1:p.Met910=
NM_001363725.1:c.480G=	NP_001350654.1:p.Met160=
XM_011535984.2:c.2811G=	XP_011534286.2:p.Met937=
XM_011535988.3:c.-20+15634G=	XP_011534290.1:n.-20+15634G=
XM_017011103.2:c.2811G=	XP_016866592.1:p.Met937=
XM_017011104.1:c.2811G=	XP_016866593.1:p.Met937=
XM_017011105.2:c.2811G=	XP_016866594.1:p.Met937=
XM_017011106.2:c.2811G=	XP_016866595.1:p.Met937=
XM_017011107.2:c.2631G=	XP_016866596.1:p.Met877=
XR_002956289.1:n.2894G=
NM_001363725.2:c.480G=	NP_001350654.1:p.Met160=
NM_001371656.1:c.3018G=	NP_001358585.1:p.Met1006=
NM_001374820.1:c.3018G=	NP_001361749.1:p.Met1006=
NM_001374828.1:c.2979G= MANE Select	NP_001361757.1:p.Met993=
NM_017519.3:c.2979G=	NP_059989.3:p.Met993=