Canonical Allele Identifier: CA366241334

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522103G>C (hg19) ; chr6:g.157200969G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200969G>C , CM000668.2:g.157200969G>C	GRCh38
NC_000006.11:g.157522103G>C , CM000668.1:g.157522103G>C	GRCh37
NC_000006.10:g.157563795G>C	NCBI36
NG_032093.1:g.428040G>C
NG_032093.2:g.428040G>C
NG_066624.1:g.429944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4585G>C	ENSP00000055163.8:p.Gly1529Arg
ENST00000414678.8:c.4654G>C	ENSP00000412835.3:p.Gly1552Arg
ENST00000637015.2:c.4873G>C	ENSP00000489729.2:p.Gly1625Arg
ENST00000346085.10:c.4624G>C	ENSP00000344546.5:p.Gly1542Arg
ENST00000350026.10:c.4336G>C	ENSP00000055163.7:p.Gly1446Arg
ENST00000414678.7:c.2902G>C	ENSP00000412835.2:p.Gly968Arg
ENST00000635849.1:c.2065G>C	ENSP00000490948.1:p.Gly689Arg
ENST00000635957.1:c.1696G>C	ENSP00000490385.1:p.Gly566Arg
ENST00000636227.1:n.3207G>C
ENST00000636254.1:n.664G>C
ENST00000636930.2:c.4744G>C MANE Select	ENSP00000490491.2:p.Gly1582Arg
ENST00000636940.1:n.2741G>C
ENST00000637015.1:c.2112G>C
ENST00000637568.1:c.2026G>C
ENST00000637741.1:n.1410G>C
ENST00000637810.1:c.2086G>C	ENSP00000489636.1:p.Gly696Arg
ENST00000637904.1:c.2245G>C	ENSP00000490550.1:p.Gly749Arg
ENST00000647938.1:c.4375G>C	ENSP00000498155.1:p.Gly1459Arg
ENST00000346085.9:c.4375G>C	ENSP00000344546.4:p.Gly1459Arg
ENST00000350026.9:c.4336G>C	ENSP00000055163.7:p.Gly1446Arg
ENST00000414678.6:c.2902G>C	ENSP00000412835.2:p.Gly968Arg
NM_017519.2:c.4336G>C	NP_059989.2:p.Gly1446Arg
NM_020732.3:c.4375G>C	NP_065783.3:p.Gly1459Arg
XM_005267069.3:c.4495G>C	XP_005267126.2:p.Gly1499Arg
XM_011535984.1:c.3574G>C	XP_011534286.1:p.Gly1192Arg
XM_011535985.1:c.3394G>C	XP_011534287.1:p.Gly1132Arg
XM_011535986.1:c.3154G>C	XP_011534288.1:p.Gly1052Arg
XM_011535987.1:c.2773G>C	XP_011534289.1:p.Gly925Arg
XM_011535988.1:c.1636G>C	XP_011534290.1:p.Gly546Arg
NM_001346813.1:c.4495G>C	NP_001333742.1:p.Gly1499Arg
NM_001363725.1:c.2245G>C	NP_001350654.1:p.Gly749Arg
XM_011535984.2:c.4705G>C	XP_011534286.2:p.Gly1569Arg
XM_011535988.3:c.1636G>C	XP_011534290.1:p.Gly546Arg
XM_017011103.2:c.4606G>C	XP_016866592.1:p.Gly1536Arg
XM_017011104.1:c.4576G>C	XP_016866593.1:p.Gly1526Arg
XM_017011105.2:c.4546G>C	XP_016866594.1:p.Gly1516Arg
XM_017011106.2:c.4417G>C	XP_016866595.1:p.Gly1473Arg
XM_017011107.2:c.4396G>C	XP_016866596.1:p.Gly1466Arg
XR_002956289.1:n.4691G>C
NM_001363725.2:c.2245G>C	NP_001350654.1:p.Gly749Arg
NM_001371656.1:c.4624G>C	NP_001358585.1:p.Gly1542Arg
NM_001374820.1:c.4624G>C	NP_001361749.1:p.Gly1542Arg
NM_001374828.1:c.4744G>C MANE Select	NP_001361757.1:p.Gly1582Arg
NM_017519.3:c.4585G>C	NP_059989.3:p.Gly1529Arg