Canonical Allele Identifier: CA366241227

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522052G>C (hg19) ; chr6:g.157200918G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200918G>C , CM000668.2:g.157200918G>C	GRCh38
NC_000006.11:g.157522052G>C , CM000668.1:g.157522052G>C	GRCh37
NC_000006.10:g.157563744G>C	NCBI36
NG_032093.1:g.427989G>C
NG_032093.2:g.427989G>C
NG_066624.1:g.429893G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4534G>C	ENSP00000055163.8:p.Gly1512Arg
ENST00000414678.8:c.4603G>C	ENSP00000412835.3:p.Gly1535Arg
ENST00000637015.2:c.4822G>C	ENSP00000489729.2:p.Gly1608Arg
ENST00000346085.10:c.4573G>C	ENSP00000344546.5:p.Gly1525Arg
ENST00000350026.10:c.4285G>C	ENSP00000055163.7:p.Gly1429Arg
ENST00000414678.7:c.2851G>C	ENSP00000412835.2:p.Gly951Arg
ENST00000635849.1:c.2014G>C	ENSP00000490948.1:p.Gly672Arg
ENST00000635957.1:c.1645G>C	ENSP00000490385.1:p.Gly549Arg
ENST00000636227.1:n.3156G>C
ENST00000636254.1:n.613G>C
ENST00000636930.2:c.4693G>C MANE Select	ENSP00000490491.2:p.Gly1565Arg
ENST00000636940.1:n.2690G>C
ENST00000637015.1:c.2061G>C
ENST00000637568.1:c.1975G>C
ENST00000637741.1:n.1359G>C
ENST00000637810.1:c.2035G>C	ENSP00000489636.1:p.Gly679Arg
ENST00000637904.1:c.2194G>C	ENSP00000490550.1:p.Gly732Arg
ENST00000647938.1:c.4324G>C	ENSP00000498155.1:p.Gly1442Arg
ENST00000346085.9:c.4324G>C	ENSP00000344546.4:p.Gly1442Arg
ENST00000350026.9:c.4285G>C	ENSP00000055163.7:p.Gly1429Arg
ENST00000414678.6:c.2851G>C	ENSP00000412835.2:p.Gly951Arg
NM_017519.2:c.4285G>C	NP_059989.2:p.Gly1429Arg
NM_020732.3:c.4324G>C	NP_065783.3:p.Gly1442Arg
XM_005267069.3:c.4444G>C	XP_005267126.2:p.Gly1482Arg
XM_011535984.1:c.3523G>C	XP_011534286.1:p.Gly1175Arg
XM_011535985.1:c.3343G>C	XP_011534287.1:p.Gly1115Arg
XM_011535986.1:c.3103G>C	XP_011534288.1:p.Gly1035Arg
XM_011535987.1:c.2722G>C	XP_011534289.1:p.Gly908Arg
XM_011535988.1:c.1585G>C	XP_011534290.1:p.Gly529Arg
NM_001346813.1:c.4444G>C	NP_001333742.1:p.Gly1482Arg
NM_001363725.1:c.2194G>C	NP_001350654.1:p.Gly732Arg
XM_011535984.2:c.4654G>C	XP_011534286.2:p.Gly1552Arg
XM_011535988.3:c.1585G>C	XP_011534290.1:p.Gly529Arg
XM_017011103.2:c.4555G>C	XP_016866592.1:p.Gly1519Arg
XM_017011104.1:c.4525G>C	XP_016866593.1:p.Gly1509Arg
XM_017011105.2:c.4495G>C	XP_016866594.1:p.Gly1499Arg
XM_017011106.2:c.4366G>C	XP_016866595.1:p.Gly1456Arg
XM_017011107.2:c.4345G>C	XP_016866596.1:p.Gly1449Arg
XR_002956289.1:n.4640G>C
NM_001363725.2:c.2194G>C	NP_001350654.1:p.Gly732Arg
NM_001371656.1:c.4573G>C	NP_001358585.1:p.Gly1525Arg
NM_001374820.1:c.4573G>C	NP_001361749.1:p.Gly1525Arg
NM_001374828.1:c.4693G>C MANE Select	NP_001361757.1:p.Gly1565Arg
NM_017519.3:c.4534G>C	NP_059989.3:p.Gly1512Arg