Canonical Allele Identifier: CA366235313

Gene: ARID1B

Linked Data

• dbSNP Id: rs747374301
• MyVariant Identifiers: chr6:g.157511254G>C (hg19) ; chr6:g.157190120G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190120G>C , CM000668.2:g.157190120G>C	GRCh38
NC_000006.11:g.157511254G>C , CM000668.1:g.157511254G>C	GRCh37
NC_000006.10:g.157552946G>C	NCBI36
NG_032093.1:g.417191G>C
NG_032093.2:g.417191G>C
NG_066624.1:g.419095G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3982G>C	ENSP00000055163.8:p.Ala1328Pro
ENST00000414678.8:c.4051G>C	ENSP00000412835.3:p.Ala1351Pro
ENST00000637015.2:c.4270G>C	ENSP00000489729.2:p.Ala1424Pro
ENST00000346085.10:c.4021G>C	ENSP00000344546.5:p.Ala1341Pro
ENST00000350026.10:c.3733G>C	ENSP00000055163.7:p.Ala1245Pro
ENST00000414678.7:c.2299G>C	ENSP00000412835.2:p.Ala767Pro
ENST00000635849.1:c.1462G>C	ENSP00000490948.1:p.Ala488Pro
ENST00000635957.1:c.1093G>C	ENSP00000490385.1:p.Ala365Pro
ENST00000636930.2:c.4141G>C MANE Select	ENSP00000490491.2:p.Ala1381Pro
ENST00000636940.1:n.2138G>C
ENST00000637015.1:c.1509G>C
ENST00000637568.1:c.1423G>C
ENST00000637741.1:n.807G>C
ENST00000637810.1:c.1483G>C	ENSP00000489636.1:p.Ala495Pro
ENST00000637904.1:c.1642G>C	ENSP00000490550.1:p.Ala548Pro
ENST00000647938.1:c.3772G>C	ENSP00000498155.1:p.Ala1258Pro
ENST00000346085.9:c.3772G>C	ENSP00000344546.4:p.Ala1258Pro
ENST00000350026.9:c.3733G>C	ENSP00000055163.7:p.Ala1245Pro
ENST00000414678.6:c.2299G>C	ENSP00000412835.2:p.Ala767Pro
NM_017519.2:c.3733G>C	NP_059989.2:p.Ala1245Pro
NM_020732.3:c.3772G>C	NP_065783.3:p.Ala1258Pro
XM_005267069.3:c.3892G>C	XP_005267126.2:p.Ala1298Pro
XM_011535984.1:c.2971G>C	XP_011534286.1:p.Ala991Pro
XM_011535985.1:c.2791G>C	XP_011534287.1:p.Ala931Pro
XM_011535986.1:c.2551G>C	XP_011534288.1:p.Ala851Pro
XM_011535987.1:c.2170G>C	XP_011534289.1:p.Ala724Pro
XM_011535988.1:c.1033G>C	XP_011534290.1:p.Ala345Pro
NM_001346813.1:c.3892G>C	NP_001333742.1:p.Ala1298Pro
NM_001363725.1:c.1642G>C	NP_001350654.1:p.Ala548Pro
XM_011535984.2:c.4102G>C	XP_011534286.2:p.Ala1368Pro
XM_011535988.3:c.1033G>C	XP_011534290.1:p.Ala345Pro
XM_017011103.2:c.4003G>C	XP_016866592.1:p.Ala1335Pro
XM_017011104.1:c.3973G>C	XP_016866593.1:p.Ala1325Pro
XM_017011105.2:c.3943G>C	XP_016866594.1:p.Ala1315Pro
XM_017011106.2:c.3814G>C	XP_016866595.1:p.Ala1272Pro
XM_017011107.2:c.3793G>C	XP_016866596.1:p.Ala1265Pro
XR_002956289.1:n.4185G>C
NM_001363725.2:c.1642G>C	NP_001350654.1:p.Ala548Pro
NM_001371656.1:c.4021G>C	NP_001358585.1:p.Ala1341Pro
NM_001374820.1:c.4021G>C	NP_001361749.1:p.Ala1341Pro
NM_001374828.1:c.4141G>C MANE Select	NP_001361757.1:p.Ala1381Pro
NM_017519.3:c.3982G>C	NP_059989.3:p.Ala1328Pro