Canonical Allele Identifier: CA452781833

Gene: ARID1B

Linked Data

• dbSNP Id: rs766441730
• gnomAD v4: 6-157190095-G-C
• MyVariant Identifiers: chr6:g.157511229G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190095G>C , CM000668.2:g.157190095G>C	GRCh38
NC_000006.11:g.157511229G>C , CM000668.1:g.157511229G>C	GRCh37
NC_000006.10:g.157552921G>C	NCBI36
NG_032093.1:g.417166G>C
NG_032093.2:g.417166G>C
NG_066624.1:g.419070G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3957G>C	ENSP00000055163.8:p.Pro1319=
ENST00000414678.8:c.4026G>C	ENSP00000412835.3:p.Pro1342=
ENST00000637015.2:c.4245G>C	ENSP00000489729.2:p.Pro1415=
ENST00000346085.10:c.3996G>C	ENSP00000344546.5:p.Pro1332=
ENST00000350026.10:c.3708G>C	ENSP00000055163.7:p.Pro1236=
ENST00000414678.7:c.2274G>C	ENSP00000412835.2:p.Pro758=
ENST00000635849.1:c.1437G>C	ENSP00000490948.1:p.Pro479=
ENST00000635957.1:c.1068G>C	ENSP00000490385.1:p.Pro356=
ENST00000636930.2:c.4116G>C MANE Select	ENSP00000490491.2:p.Pro1372=
ENST00000636940.1:n.2113G>C
ENST00000637015.1:c.1484G>C
ENST00000637568.1:c.1398G>C
ENST00000637741.1:n.782G>C
ENST00000637810.1:c.1458G>C	ENSP00000489636.1:p.Pro486=
ENST00000637904.1:c.1617G>C	ENSP00000490550.1:p.Pro539=
ENST00000647938.1:c.3747G>C	ENSP00000498155.1:p.Pro1249=
ENST00000346085.9:c.3747G>C	ENSP00000344546.4:p.Pro1249=
ENST00000350026.9:c.3708G>C	ENSP00000055163.7:p.Pro1236=
ENST00000414678.6:c.2274G>C	ENSP00000412835.2:p.Pro758=
NM_017519.2:c.3708G>C	NP_059989.2:p.Pro1236=
NM_020732.3:c.3747G>C	NP_065783.3:p.Pro1249=
XM_005267069.3:c.3867G>C	XP_005267126.2:p.Pro1289=
XM_011535984.1:c.2946G>C	XP_011534286.1:p.Pro982=
XM_011535985.1:c.2766G>C	XP_011534287.1:p.Pro922=
XM_011535986.1:c.2526G>C	XP_011534288.1:p.Pro842=
XM_011535987.1:c.2145G>C	XP_011534289.1:p.Pro715=
XM_011535988.1:c.1008G>C	XP_011534290.1:p.Pro336=
NM_001346813.1:c.3867G>C	NP_001333742.1:p.Pro1289=
NM_001363725.1:c.1617G>C	NP_001350654.1:p.Pro539=
XM_011535984.2:c.4077G>C	XP_011534286.2:p.Pro1359=
XM_011535988.3:c.1008G>C	XP_011534290.1:p.Pro336=
XM_017011103.2:c.3978G>C	XP_016866592.1:p.Pro1326=
XM_017011104.1:c.3948G>C	XP_016866593.1:p.Pro1316=
XM_017011105.2:c.3918G>C	XP_016866594.1:p.Pro1306=
XM_017011106.2:c.3789G>C	XP_016866595.1:p.Pro1263=
XM_017011107.2:c.3768G>C	XP_016866596.1:p.Pro1256=
XR_002956289.1:n.4160G>C
NM_001363725.2:c.1617G>C	NP_001350654.1:p.Pro539=
NM_001371656.1:c.3996G>C	NP_001358585.1:p.Pro1332=
NM_001374820.1:c.3996G>C	NP_001361749.1:p.Pro1332=
NM_001374828.1:c.4116G>C MANE Select	NP_001361757.1:p.Pro1372=
NM_017519.3:c.3957G>C	NP_059989.3:p.Pro1319=