Canonical Allele Identifier: CA452780776

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157181080-A-C
• MyVariant Identifiers: chr6:g.157502214A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181080A>C , CM000668.2:g.157181080A>C	GRCh38
NC_000006.11:g.157502214A>C , CM000668.1:g.157502214A>C	GRCh37
NC_000006.10:g.157543906A>C	NCBI36
NG_032093.1:g.408151A>C
NG_032093.2:g.408151A>C
NG_066624.1:g.410055A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3457A>C	ENSP00000055163.8:p.Arg1153=
ENST00000414678.8:c.3526A>C	ENSP00000412835.3:p.Arg1176=
ENST00000637015.2:c.3745A>C	ENSP00000489729.2:p.Arg1249=
ENST00000319584.11:c.1630A>C	ENSP00000313006.7:p.Arg544=
ENST00000346085.10:c.3496A>C	ENSP00000344546.5:p.Arg1166=
ENST00000350026.10:c.3208A>C	ENSP00000055163.7:p.Arg1070=
ENST00000414678.7:c.1774A>C	ENSP00000412835.2:p.Arg592=
ENST00000635849.1:c.937A>C	ENSP00000490948.1:p.Arg313=
ENST00000635957.1:c.571A>C	ENSP00000490385.1:p.Arg191=
ENST00000636930.2:c.3616A>C MANE Select	ENSP00000490491.2:p.Arg1206=
ENST00000636940.1:n.1613A>C
ENST00000637015.1:c.984A>C
ENST00000637568.1:c.898A>C
ENST00000637741.1:n.282A>C
ENST00000637810.1:c.958A>C	ENSP00000489636.1:p.Arg320=
ENST00000637904.1:c.1117A>C	ENSP00000490550.1:p.Arg373=
ENST00000647938.1:c.3247A>C	ENSP00000498155.1:p.Arg1083=
ENST00000319584.10:c.1633A>C	ENSP00000313006.6:p.Arg545=
ENST00000346085.9:c.3247A>C	ENSP00000344546.4:p.Arg1083=
ENST00000350026.9:c.3208A>C	ENSP00000055163.7:p.Arg1070=
ENST00000400790.3:c.409A>C	ENSP00000383596.3:p.Arg137=
ENST00000414678.6:c.1774A>C	ENSP00000412835.2:p.Arg592=
ENST00000478761.3:c.818A>C
NM_017519.2:c.3208A>C	NP_059989.2:p.Arg1070=
NM_020732.3:c.3247A>C	NP_065783.3:p.Arg1083=
XM_005267069.3:c.3367A>C	XP_005267126.2:p.Arg1123=
XM_011535984.1:c.2446A>C	XP_011534286.1:p.Arg816=
XM_011535985.1:c.2266A>C	XP_011534287.1:p.Arg756=
XM_011535986.1:c.2026A>C	XP_011534288.1:p.Arg676=
XM_011535987.1:c.1645A>C	XP_011534289.1:p.Arg549=
XM_011535988.1:c.508A>C	XP_011534290.1:p.Arg170=
NM_001346813.1:c.3367A>C	NP_001333742.1:p.Arg1123=
NM_001363725.1:c.1117A>C	NP_001350654.1:p.Arg373=
XM_011535984.2:c.3577A>C	XP_011534286.2:p.Arg1193=
XM_011535988.3:c.508A>C	XP_011534290.1:p.Arg170=
XM_017011103.2:c.3478A>C	XP_016866592.1:p.Arg1160=
XM_017011104.1:c.3448A>C	XP_016866593.1:p.Arg1150=
XM_017011105.2:c.3418A>C	XP_016866594.1:p.Arg1140=
XM_017011106.2:c.3289A>C	XP_016866595.1:p.Arg1097=
XM_017011107.2:c.3268A>C	XP_016866596.1:p.Arg1090=
XR_002956289.1:n.3660A>C
NM_001363725.2:c.1117A>C	NP_001350654.1:p.Arg373=
NM_001371656.1:c.3496A>C	NP_001358585.1:p.Arg1166=
NM_001374820.1:c.3496A>C	NP_001361749.1:p.Arg1166=
NM_001374828.1:c.3616A>C MANE Select	NP_001361757.1:p.Arg1206=
NM_017519.3:c.3457A>C	NP_059989.3:p.Arg1153=