Canonical Allele Identifier: CA366235314

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190120-G-T
• MyVariant Identifiers: chr6:g.157511254G>T (hg19) ; chr6:g.157190120G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3982G>T	ENSP00000055163.8:p.Ala1328Ser
ENST00000414678.8:c.4051G>T	ENSP00000412835.3:p.Ala1351Ser
ENST00000637015.2:c.4270G>T	ENSP00000489729.2:p.Ala1424Ser
ENST00000346085.10:c.4021G>T	ENSP00000344546.5:p.Ala1341Ser
ENST00000350026.10:c.3733G>T	ENSP00000055163.7:p.Ala1245Ser
ENST00000414678.7:c.2299G>T	ENSP00000412835.2:p.Ala767Ser
ENST00000635849.1:c.1462G>T	ENSP00000490948.1:p.Ala488Ser
ENST00000635957.1:c.1093G>T	ENSP00000490385.1:p.Ala365Ser
ENST00000636930.2:c.4141G>T MANE Select	ENSP00000490491.2:p.Ala1381Ser
ENST00000636940.1:n.2138G>T
ENST00000637015.1:c.1509G>T
ENST00000637568.1:c.1423G>T
ENST00000637741.1:n.807G>T
ENST00000637810.1:c.1483G>T	ENSP00000489636.1:p.Ala495Ser
ENST00000637904.1:c.1642G>T	ENSP00000490550.1:p.Ala548Ser
ENST00000647938.1:c.3772G>T	ENSP00000498155.1:p.Ala1258Ser
ENST00000346085.9:c.3772G>T	ENSP00000344546.4:p.Ala1258Ser
ENST00000350026.9:c.3733G>T	ENSP00000055163.7:p.Ala1245Ser
ENST00000414678.6:c.2299G>T	ENSP00000412835.2:p.Ala767Ser
NM_017519.2:c.3733G>T	NP_059989.2:p.Ala1245Ser
NM_020732.3:c.3772G>T	NP_065783.3:p.Ala1258Ser
XM_005267069.3:c.3892G>T	XP_005267126.2:p.Ala1298Ser
XM_011535984.1:c.2971G>T	XP_011534286.1:p.Ala991Ser
XM_011535985.1:c.2791G>T	XP_011534287.1:p.Ala931Ser
XM_011535986.1:c.2551G>T	XP_011534288.1:p.Ala851Ser
XM_011535987.1:c.2170G>T	XP_011534289.1:p.Ala724Ser
XM_011535988.1:c.1033G>T	XP_011534290.1:p.Ala345Ser
NM_001346813.1:c.3892G>T	NP_001333742.1:p.Ala1298Ser
NM_001363725.1:c.1642G>T	NP_001350654.1:p.Ala548Ser
XM_011535984.2:c.4102G>T	XP_011534286.2:p.Ala1368Ser
XM_011535988.3:c.1033G>T	XP_011534290.1:p.Ala345Ser
XM_017011103.2:c.4003G>T	XP_016866592.1:p.Ala1335Ser
XM_017011104.1:c.3973G>T	XP_016866593.1:p.Ala1325Ser
XM_017011105.2:c.3943G>T	XP_016866594.1:p.Ala1315Ser
XM_017011106.2:c.3814G>T	XP_016866595.1:p.Ala1272Ser
XM_017011107.2:c.3793G>T	XP_016866596.1:p.Ala1265Ser
XR_002956289.1:n.4185G>T
NM_001363725.2:c.1642G>T	NP_001350654.1:p.Ala548Ser
NM_001371656.1:c.4021G>T	NP_001358585.1:p.Ala1341Ser
NM_001374820.1:c.4021G>T	NP_001361749.1:p.Ala1341Ser
NM_001374828.1:c.4141G>T MANE Select	NP_001361757.1:p.Ala1381Ser
NM_017519.3:c.3982G>T	NP_059989.3:p.Ala1328Ser