Canonical Allele Identifier: CA366242775

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376296
• MyVariant Identifiers: chr6:g.157522502G>C (hg19) ; chr6:g.157201368G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201368G>C , CM000668.2:g.157201368G>C	GRCh38
NC_000006.11:g.157522502G>C , CM000668.1:g.157522502G>C	GRCh37
NC_000006.10:g.157564194G>C	NCBI36
NG_032093.1:g.428439G>C
NG_032093.2:g.428439G>C
NG_066624.1:g.430343G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4984G>C	ENSP00000055163.8:p.Val1662Leu
ENST00000414678.8:c.5053G>C	ENSP00000412835.3:p.Val1685Leu
ENST00000637015.2:c.5272G>C	ENSP00000489729.2:p.Val1758Leu
ENST00000346085.10:c.5023G>C	ENSP00000344546.5:p.Val1675Leu
ENST00000350026.10:c.4735G>C	ENSP00000055163.7:p.Val1579Leu
ENST00000414678.7:c.3301G>C	ENSP00000412835.2:p.Val1101Leu
ENST00000635849.1:c.2464G>C	ENSP00000490948.1:p.Val822Leu
ENST00000635957.1:c.2095G>C	ENSP00000490385.1:p.Val699Leu
ENST00000636227.1:n.3606G>C
ENST00000636254.1:n.1063G>C
ENST00000636930.2:c.5143G>C MANE Select	ENSP00000490491.2:p.Val1715Leu
ENST00000636940.1:n.3140G>C
ENST00000637015.1:c.2511G>C
ENST00000637568.1:c.2425G>C
ENST00000637741.1:n.1809G>C
ENST00000637810.1:c.2485G>C	ENSP00000489636.1:p.Val829Leu
ENST00000637904.1:c.2644G>C	ENSP00000490550.1:p.Val882Leu
ENST00000647938.1:c.4774G>C	ENSP00000498155.1:p.Val1592Leu
ENST00000346085.9:c.4774G>C	ENSP00000344546.4:p.Val1592Leu
ENST00000350026.9:c.4735G>C	ENSP00000055163.7:p.Val1579Leu
ENST00000414678.6:c.3301G>C	ENSP00000412835.2:p.Val1101Leu
NM_017519.2:c.4735G>C	NP_059989.2:p.Val1579Leu
NM_020732.3:c.4774G>C	NP_065783.3:p.Val1592Leu
XM_005267069.3:c.4894G>C	XP_005267126.2:p.Val1632Leu
XM_011535984.1:c.3973G>C	XP_011534286.1:p.Val1325Leu
XM_011535985.1:c.3793G>C	XP_011534287.1:p.Val1265Leu
XM_011535986.1:c.3553G>C	XP_011534288.1:p.Val1185Leu
XM_011535987.1:c.3172G>C	XP_011534289.1:p.Val1058Leu
XM_011535988.1:c.2035G>C	XP_011534290.1:p.Val679Leu
NM_001346813.1:c.4894G>C	NP_001333742.1:p.Val1632Leu
NM_001363725.1:c.2644G>C	NP_001350654.1:p.Val882Leu
XM_011535984.2:c.5104G>C	XP_011534286.2:p.Val1702Leu
XM_011535988.3:c.2035G>C	XP_011534290.1:p.Val679Leu
XM_017011103.2:c.5005G>C	XP_016866592.1:p.Val1669Leu
XM_017011104.1:c.4975G>C	XP_016866593.1:p.Val1659Leu
XM_017011105.2:c.4945G>C	XP_016866594.1:p.Val1649Leu
XM_017011106.2:c.4816G>C	XP_016866595.1:p.Val1606Leu
XM_017011107.2:c.4795G>C	XP_016866596.1:p.Val1599Leu
XR_002956289.1:n.5090G>C
NM_001363725.2:c.2644G>C	NP_001350654.1:p.Val882Leu
NM_001371656.1:c.5023G>C	NP_001358585.1:p.Val1675Leu
NM_001374820.1:c.5023G>C	NP_001361749.1:p.Val1675Leu
NM_001374828.1:c.5143G>C MANE Select	NP_001361757.1:p.Val1715Leu
NM_017519.3:c.4984G>C	NP_059989.3:p.Val1662Leu