Canonical Allele Identifier: CA452780750

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157181034-A-C
• MyVariant Identifiers: chr6:g.157502168A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181034A>C , CM000668.2:g.157181034A>C	GRCh38
NC_000006.11:g.157502168A>C , CM000668.1:g.157502168A>C	GRCh37
NC_000006.10:g.157543860A>C	NCBI36
NG_032093.1:g.408105A>C
NG_032093.2:g.408105A>C
NG_066624.1:g.410009A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3411A>C	ENSP00000055163.8:p.Pro1137=
ENST00000414678.8:c.3480A>C	ENSP00000412835.3:p.Pro1160=
ENST00000637015.2:c.3699A>C	ENSP00000489729.2:p.Pro1233=
ENST00000319584.11:c.1584A>C	ENSP00000313006.7:p.Pro528=
ENST00000346085.10:c.3450A>C	ENSP00000344546.5:p.Pro1150=
ENST00000350026.10:c.3162A>C	ENSP00000055163.7:p.Pro1054=
ENST00000414678.7:c.1728A>C	ENSP00000412835.2:p.Pro576=
ENST00000635849.1:c.891A>C	ENSP00000490948.1:p.Pro297=
ENST00000635957.1:c.525A>C	ENSP00000490385.1:p.Pro175=
ENST00000636930.2:c.3570A>C MANE Select	ENSP00000490491.2:p.Pro1190=
ENST00000636940.1:n.1567A>C
ENST00000637015.1:c.938A>C
ENST00000637568.1:c.852A>C
ENST00000637741.1:n.236A>C
ENST00000637810.1:c.912A>C	ENSP00000489636.1:p.Pro304=
ENST00000637904.1:c.1071A>C	ENSP00000490550.1:p.Pro357=
ENST00000647938.1:c.3201A>C	ENSP00000498155.1:p.Pro1067=
ENST00000319584.10:c.1587A>C	ENSP00000313006.6:p.Pro529=
ENST00000346085.9:c.3201A>C	ENSP00000344546.4:p.Pro1067=
ENST00000350026.9:c.3162A>C	ENSP00000055163.7:p.Pro1054=
ENST00000400790.3:c.363A>C	ENSP00000383596.3:p.Pro121=
ENST00000414678.6:c.1728A>C	ENSP00000412835.2:p.Pro576=
ENST00000478761.3:c.772A>C
NM_017519.2:c.3162A>C	NP_059989.2:p.Pro1054=
NM_020732.3:c.3201A>C	NP_065783.3:p.Pro1067=
XM_005267069.3:c.3321A>C	XP_005267126.2:p.Pro1107=
XM_011535984.1:c.2400A>C	XP_011534286.1:p.Pro800=
XM_011535985.1:c.2220A>C	XP_011534287.1:p.Pro740=
XM_011535986.1:c.1980A>C	XP_011534288.1:p.Pro660=
XM_011535987.1:c.1599A>C	XP_011534289.1:p.Pro533=
XM_011535988.1:c.462A>C	XP_011534290.1:p.Pro154=
NM_001346813.1:c.3321A>C	NP_001333742.1:p.Pro1107=
NM_001363725.1:c.1071A>C	NP_001350654.1:p.Pro357=
XM_011535984.2:c.3531A>C	XP_011534286.2:p.Pro1177=
XM_011535988.3:c.462A>C	XP_011534290.1:p.Pro154=
XM_017011103.2:c.3432A>C	XP_016866592.1:p.Pro1144=
XM_017011104.1:c.3402A>C	XP_016866593.1:p.Pro1134=
XM_017011105.2:c.3372A>C	XP_016866594.1:p.Pro1124=
XM_017011106.2:c.3243A>C	XP_016866595.1:p.Pro1081=
XM_017011107.2:c.3222A>C	XP_016866596.1:p.Pro1074=
XR_002956289.1:n.3614A>C
NM_001363725.2:c.1071A>C	NP_001350654.1:p.Pro357=
NM_001371656.1:c.3450A>C	NP_001358585.1:p.Pro1150=
NM_001374820.1:c.3450A>C	NP_001361749.1:p.Pro1150=
NM_001374828.1:c.3570A>C MANE Select	NP_001361757.1:p.Pro1190=
NM_017519.3:c.3411A>C	NP_059989.3:p.Pro1137=