Canonical Allele Identifier: CA16042664

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148848C>T , CM000668.2:g.157148848C>T	GRCh38
NC_000006.11:g.157469982C>T , CM000668.1:g.157469982C>T	GRCh37
NC_000006.10:g.157511674C>T	NCBI36
NG_032093.1:g.375919C>T
NG_032093.2:g.375919C>T
NG_066624.1:g.377823C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2986C>T	ENSP00000055163.8:p.Gln996Ter
ENST00000414678.8:c.2896C>T	ENSP00000412835.3:p.Gln966Ter
ENST00000637015.2:c.2986C>T	ENSP00000489729.2:p.Gln996Ter
ENST00000319584.11:c.1000C>T	ENSP00000313006.7:p.Gln334Ter
ENST00000346085.10:c.3025C>T	ENSP00000344546.5:p.Gln1009Ter
ENST00000350026.10:c.2737C>T	ENSP00000055163.7:p.Gln913Ter
ENST00000414678.7:c.1144C>T	ENSP00000412835.2:p.Gln382Ter
ENST00000452544.2:n.887C>T
ENST00000635849.1:c.307C>T	ENSP00000490948.1:p.Gln103Ter
ENST00000636426.1:n.120C>T
ENST00000636930.2:c.2986C>T MANE Select	ENSP00000490491.2:p.Gln996Ter
ENST00000637015.1:c.225C>T
ENST00000637568.1:c.29C>T
ENST00000637810.1:c.487C>T	ENSP00000489636.1:p.Gln163Ter
ENST00000637904.1:c.487C>T	ENSP00000490550.1:p.Gln163Ter
ENST00000647938.1:c.2776C>T	ENSP00000498155.1:p.Gln926Ter
ENST00000674190.1:n.1735C>T
ENST00000319584.10:c.1003C>T	ENSP00000313006.6:p.Gln335Ter
ENST00000346085.9:c.2776C>T	ENSP00000344546.4:p.Gln926Ter
ENST00000350026.9:c.2737C>T	ENSP00000055163.7:p.Gln913Ter
ENST00000414678.6:c.1144C>T	ENSP00000412835.2:p.Gln382Ter
ENST00000452544.1:n.833C>T
ENST00000478761.3:c.59C>T
NM_017519.2:c.2737C>T	NP_059989.2:p.Gln913Ter
NM_020732.3:c.2776C>T	NP_065783.3:p.Gln926Ter
XM_005267069.3:c.2737C>T	XP_005267126.2:p.Gln913Ter
XM_011535984.1:c.1687C>T	XP_011534286.1:p.Gln563Ter
XM_011535985.1:c.1507C>T	XP_011534287.1:p.Gln503Ter
XM_011535986.1:c.1267C>T	XP_011534288.1:p.Gln423Ter
XM_011535987.1:c.886C>T	XP_011534289.1:p.Gln296Ter
XM_011535988.1:c.-20+15641C>T	XP_011534290.1:n.-20+15641C>T
NM_001346813.1:c.2737C>T	NP_001333742.1:p.Gln913Ter
NM_001363725.1:c.487C>T	NP_001350654.1:p.Gln163Ter
XM_011535984.2:c.2818C>T	XP_011534286.2:p.Gln940Ter
XM_011535988.3:c.-20+15641C>T	XP_011534290.1:n.-20+15641C>T
XM_017011103.2:c.2818C>T	XP_016866592.1:p.Gln940Ter
XM_017011104.1:c.2818C>T	XP_016866593.1:p.Gln940Ter
XM_017011105.2:c.2818C>T	XP_016866594.1:p.Gln940Ter
XM_017011106.2:c.2818C>T	XP_016866595.1:p.Gln940Ter
XM_017011107.2:c.2638C>T	XP_016866596.1:p.Gln880Ter
XR_002956289.1:n.2901C>T
NM_001363725.2:c.487C>T	NP_001350654.1:p.Gln163Ter
NM_001371656.1:c.3025C>T	NP_001358585.1:p.Gln1009Ter
NM_001374820.1:c.3025C>T	NP_001361749.1:p.Gln1009Ter
NM_001374828.1:c.2986C>T MANE Select	NP_001361757.1:p.Gln996Ter
NM_017519.3:c.2986C>T	NP_059989.3:p.Gln996Ter