Canonical Allele Identifier: CA366384574

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128046967
• MyVariant Identifiers: chr6:g.157150515C>T (hg19) ; chr6:g.156829381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829381C>T , CM000668.2:g.156829381C>T	GRCh38
NC_000006.11:g.157150515C>T , CM000668.1:g.157150515C>T	GRCh37
NC_000006.10:g.157192207C>T	NCBI36
NG_032093.1:g.56452C>T
NG_032093.2:g.56452C>T
NG_066624.1:g.58356C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.1946C>T	ENSP00000055163.8:p.Thr649Ile
ENST00000414678.8:c.1946C>T	ENSP00000412835.3:p.Thr649Ile
ENST00000637015.2:c.1946C>T	ENSP00000489729.2:p.Thr649Ile
ENST00000346085.10:c.1946C>T	ENSP00000344546.5:p.Thr649Ile
ENST00000350026.10:c.1697C>T	ENSP00000055163.7:p.Thr566Ile
ENST00000414678.7:c.194C>T	ENSP00000412835.2:p.Thr65Ile
ENST00000494260.2:c.227C>T	ENSP00000490094.1:p.Thr76Ile
ENST00000636205.1:n.9C>T
ENST00000636607.1:c.209C>T	ENSP00000490050.1:p.Thr70Ile
ENST00000636748.1:c.227C>T	ENSP00000489917.1:p.Thr76Ile
ENST00000636930.2:c.1946C>T MANE Select	ENSP00000490491.2:p.Thr649Ile
ENST00000637910.1:n.227C>T
ENST00000638000.1:c.163C>T
ENST00000647938.1:c.1697C>T	ENSP00000498155.1:p.Thr566Ile
ENST00000674190.1:n.653C>T
ENST00000674298.1:c.1686C>T
ENST00000346085.9:c.1697C>T	ENSP00000344546.4:p.Thr566Ile
ENST00000350026.9:c.1697C>T	ENSP00000055163.7:p.Thr566Ile
ENST00000414678.6:c.194C>T	ENSP00000412835.2:p.Thr65Ile
ENST00000494260.1:n.155C>T
NM_017519.2:c.1697C>T	NP_059989.2:p.Thr566Ile
NM_020732.3:c.1697C>T	NP_065783.3:p.Thr566Ile
XM_005267069.3:c.1697C>T	XP_005267126.2:p.Thr566Ile
XM_011535984.1:c.566C>T	XP_011534286.1:p.Thr189Ile
XM_011535985.1:c.566C>T	XP_011534287.1:p.Thr189Ile
XM_011535986.1:c.146C>T	XP_011534288.1:p.Thr49Ile
NM_001346813.1:c.1697C>T	NP_001333742.1:p.Thr566Ile
XM_011535984.2:c.1697C>T	XP_011534286.2:p.Thr566Ile
XM_017011103.2:c.1697C>T	XP_016866592.1:p.Thr566Ile
XM_017011104.1:c.1697C>T	XP_016866593.1:p.Thr566Ile
XM_017011105.2:c.1697C>T	XP_016866594.1:p.Thr566Ile
XM_017011106.2:c.1697C>T	XP_016866595.1:p.Thr566Ile
XM_017011107.2:c.1697C>T	XP_016866596.1:p.Thr566Ile
XR_002956289.1:n.1780C>T
NM_001371656.1:c.1946C>T	NP_001358585.1:p.Thr649Ile
NM_001374820.1:c.1946C>T	NP_001361749.1:p.Thr649Ile
NM_001374828.1:c.1946C>T MANE Select	NP_001361757.1:p.Thr649Ile
NM_017519.3:c.1946C>T	NP_059989.3:p.Thr649Ile