Canonical Allele Identifier: CA452990274

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148829-T-C
• MyVariant Identifiers: chr6:g.157469963T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148829T>C , CM000668.2:g.157148829T>C	GRCh38
NC_000006.11:g.157469963T>C , CM000668.1:g.157469963T>C	GRCh37
NC_000006.10:g.157511655T>C	NCBI36
NG_032093.1:g.375900T>C
NG_032093.2:g.375900T>C
NG_066624.1:g.377804T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2967T>C	ENSP00000055163.8:p.Ser989=
ENST00000414678.8:c.2877T>C	ENSP00000412835.3:p.Ser959=
ENST00000637015.2:c.2967T>C	ENSP00000489729.2:p.Ser989=
ENST00000319584.11:c.981T>C	ENSP00000313006.7:p.Ser327=
ENST00000346085.10:c.3006T>C	ENSP00000344546.5:p.Ser1002=
ENST00000350026.10:c.2718T>C	ENSP00000055163.7:p.Ser906=
ENST00000414678.7:c.1125T>C	ENSP00000412835.2:p.Ser375=
ENST00000452544.2:n.868T>C
ENST00000635849.1:c.288T>C	ENSP00000490948.1:p.Ser96=
ENST00000636426.1:n.101T>C
ENST00000636930.2:c.2967T>C MANE Select	ENSP00000490491.2:p.Ser989=
ENST00000637015.1:c.206T>C
ENST00000637568.1:c.10T>C
ENST00000637810.1:c.468T>C	ENSP00000489636.1:p.Ser156=
ENST00000637904.1:c.468T>C	ENSP00000490550.1:p.Ser156=
ENST00000647938.1:c.2757T>C	ENSP00000498155.1:p.Ser919=
ENST00000674190.1:n.1716T>C
ENST00000319584.10:c.984T>C	ENSP00000313006.6:p.Ser328=
ENST00000346085.9:c.2757T>C	ENSP00000344546.4:p.Ser919=
ENST00000350026.9:c.2718T>C	ENSP00000055163.7:p.Ser906=
ENST00000414678.6:c.1125T>C	ENSP00000412835.2:p.Ser375=
ENST00000452544.1:n.814T>C
ENST00000478761.3:c.40T>C
NM_017519.2:c.2718T>C	NP_059989.2:p.Ser906=
NM_020732.3:c.2757T>C	NP_065783.3:p.Ser919=
XM_005267069.3:c.2718T>C	XP_005267126.2:p.Ser906=
XM_011535984.1:c.1668T>C	XP_011534286.1:p.Ser556=
XM_011535985.1:c.1488T>C	XP_011534287.1:p.Ser496=
XM_011535986.1:c.1248T>C	XP_011534288.1:p.Ser416=
XM_011535987.1:c.867T>C	XP_011534289.1:p.Ser289=
XM_011535988.1:c.-20+15622T>C	XP_011534290.1:n.-20+15622T>C
NM_001346813.1:c.2718T>C	NP_001333742.1:p.Ser906=
NM_001363725.1:c.468T>C	NP_001350654.1:p.Ser156=
XM_011535984.2:c.2799T>C	XP_011534286.2:p.Ser933=
XM_011535988.3:c.-20+15622T>C	XP_011534290.1:n.-20+15622T>C
XM_017011103.2:c.2799T>C	XP_016866592.1:p.Ser933=
XM_017011104.1:c.2799T>C	XP_016866593.1:p.Ser933=
XM_017011105.2:c.2799T>C	XP_016866594.1:p.Ser933=
XM_017011106.2:c.2799T>C	XP_016866595.1:p.Ser933=
XM_017011107.2:c.2619T>C	XP_016866596.1:p.Ser873=
XR_002956289.1:n.2882T>C
NM_001363725.2:c.468T>C	NP_001350654.1:p.Ser156=
NM_001371656.1:c.3006T>C	NP_001358585.1:p.Ser1002=
NM_001374820.1:c.3006T>C	NP_001361749.1:p.Ser1002=
NM_001374828.1:c.2967T>C MANE Select	NP_001361757.1:p.Ser989=
NM_017519.3:c.2967T>C	NP_059989.3:p.Ser989=