Canonical Allele Identifier: CA452784785

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376387
• gnomAD v4: 6-157201376-G-C
• MyVariant Identifiers: chr6:g.157522510G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201376G>C , CM000668.2:g.157201376G>C	GRCh38
NC_000006.11:g.157522510G>C , CM000668.1:g.157522510G>C	GRCh37
NC_000006.10:g.157564202G>C	NCBI36
NG_032093.1:g.428447G>C
NG_032093.2:g.428447G>C
NG_066624.1:g.430351G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4992G>C	ENSP00000055163.8:p.Gly1664=
ENST00000414678.8:c.5061G>C	ENSP00000412835.3:p.Gly1687=
ENST00000637015.2:c.5280G>C	ENSP00000489729.2:p.Gly1760=
ENST00000346085.10:c.5031G>C	ENSP00000344546.5:p.Gly1677=
ENST00000350026.10:c.4743G>C	ENSP00000055163.7:p.Gly1581=
ENST00000414678.7:c.3309G>C	ENSP00000412835.2:p.Gly1103=
ENST00000635849.1:c.2472G>C	ENSP00000490948.1:p.Gly824=
ENST00000635957.1:c.2103G>C	ENSP00000490385.1:p.Gly701=
ENST00000636227.1:n.3614G>C
ENST00000636254.1:n.1071G>C
ENST00000636930.2:c.5151G>C MANE Select	ENSP00000490491.2:p.Gly1717=
ENST00000636940.1:n.3148G>C
ENST00000637015.1:c.2519G>C
ENST00000637568.1:c.2433G>C
ENST00000637741.1:n.1817G>C
ENST00000637810.1:c.2493G>C	ENSP00000489636.1:p.Gly831=
ENST00000637904.1:c.2652G>C	ENSP00000490550.1:p.Gly884=
ENST00000647938.1:c.4782G>C	ENSP00000498155.1:p.Gly1594=
ENST00000346085.9:c.4782G>C	ENSP00000344546.4:p.Gly1594=
ENST00000350026.9:c.4743G>C	ENSP00000055163.7:p.Gly1581=
ENST00000414678.6:c.3309G>C	ENSP00000412835.2:p.Gly1103=
NM_017519.2:c.4743G>C	NP_059989.2:p.Gly1581=
NM_020732.3:c.4782G>C	NP_065783.3:p.Gly1594=
XM_005267069.3:c.4902G>C	XP_005267126.2:p.Gly1634=
XM_011535984.1:c.3981G>C	XP_011534286.1:p.Gly1327=
XM_011535985.1:c.3801G>C	XP_011534287.1:p.Gly1267=
XM_011535986.1:c.3561G>C	XP_011534288.1:p.Gly1187=
XM_011535987.1:c.3180G>C	XP_011534289.1:p.Gly1060=
XM_011535988.1:c.2043G>C	XP_011534290.1:p.Gly681=
NM_001346813.1:c.4902G>C	NP_001333742.1:p.Gly1634=
NM_001363725.1:c.2652G>C	NP_001350654.1:p.Gly884=
XM_011535984.2:c.5112G>C	XP_011534286.2:p.Gly1704=
XM_011535988.3:c.2043G>C	XP_011534290.1:p.Gly681=
XM_017011103.2:c.5013G>C	XP_016866592.1:p.Gly1671=
XM_017011104.1:c.4983G>C	XP_016866593.1:p.Gly1661=
XM_017011105.2:c.4953G>C	XP_016866594.1:p.Gly1651=
XM_017011106.2:c.4824G>C	XP_016866595.1:p.Gly1608=
XM_017011107.2:c.4803G>C	XP_016866596.1:p.Gly1601=
XR_002956289.1:n.5098G>C
NM_001363725.2:c.2652G>C	NP_001350654.1:p.Gly884=
NM_001371656.1:c.5031G>C	NP_001358585.1:p.Gly1677=
NM_001374820.1:c.5031G>C	NP_001361749.1:p.Gly1677=
NM_001374828.1:c.5151G>C MANE Select	NP_001361757.1:p.Gly1717=
NM_017519.3:c.4992G>C	NP_059989.3:p.Gly1664=