Canonical Allele Identifier: CA452990242

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634562
• MyVariant Identifiers: chr6:g.157469948C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148814C>T , CM000668.2:g.157148814C>T	GRCh38
NC_000006.11:g.157469948C>T , CM000668.1:g.157469948C>T	GRCh37
NC_000006.10:g.157511640C>T	NCBI36
NG_032093.1:g.375885C>T
NG_032093.2:g.375885C>T
NG_066624.1:g.377789C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2952C>T	ENSP00000055163.8:p.Ser984=
ENST00000414678.8:c.2862C>T	ENSP00000412835.3:p.Ser954=
ENST00000637015.2:c.2952C>T	ENSP00000489729.2:p.Ser984=
ENST00000319584.11:c.966C>T	ENSP00000313006.7:p.Ser322=
ENST00000346085.10:c.2991C>T	ENSP00000344546.5:p.Ser997=
ENST00000350026.10:c.2703C>T	ENSP00000055163.7:p.Ser901=
ENST00000414678.7:c.1110C>T	ENSP00000412835.2:p.Ser370=
ENST00000452544.2:n.853C>T
ENST00000635849.1:c.273C>T	ENSP00000490948.1:p.Ser91=
ENST00000636426.1:n.86C>T
ENST00000636930.2:c.2952C>T MANE Select	ENSP00000490491.2:p.Ser984=
ENST00000637015.1:c.191C>T
ENST00000637810.1:c.453C>T	ENSP00000489636.1:p.Ser151=
ENST00000637904.1:c.453C>T	ENSP00000490550.1:p.Ser151=
ENST00000647938.1:c.2742C>T	ENSP00000498155.1:p.Ser914=
ENST00000674190.1:n.1701C>T
ENST00000319584.10:c.969C>T	ENSP00000313006.6:p.Ser323=
ENST00000346085.9:c.2742C>T	ENSP00000344546.4:p.Ser914=
ENST00000350026.9:c.2703C>T	ENSP00000055163.7:p.Ser901=
ENST00000414678.6:c.1110C>T	ENSP00000412835.2:p.Ser370=
ENST00000452544.1:n.799C>T
ENST00000478761.3:c.25C>T
NM_017519.2:c.2703C>T	NP_059989.2:p.Ser901=
NM_020732.3:c.2742C>T	NP_065783.3:p.Ser914=
XM_005267069.3:c.2703C>T	XP_005267126.2:p.Ser901=
XM_011535984.1:c.1653C>T	XP_011534286.1:p.Ser551=
XM_011535985.1:c.1473C>T	XP_011534287.1:p.Ser491=
XM_011535986.1:c.1233C>T	XP_011534288.1:p.Ser411=
XM_011535987.1:c.852C>T	XP_011534289.1:p.Ser284=
XM_011535988.1:c.-20+15607C>T	XP_011534290.1:n.-20+15607C>T
NM_001346813.1:c.2703C>T	NP_001333742.1:p.Ser901=
NM_001363725.1:c.453C>T	NP_001350654.1:p.Ser151=
XM_011535984.2:c.2784C>T	XP_011534286.2:p.Ser928=
XM_011535988.3:c.-20+15607C>T	XP_011534290.1:n.-20+15607C>T
XM_017011103.2:c.2784C>T	XP_016866592.1:p.Ser928=
XM_017011104.1:c.2784C>T	XP_016866593.1:p.Ser928=
XM_017011105.2:c.2784C>T	XP_016866594.1:p.Ser928=
XM_017011106.2:c.2784C>T	XP_016866595.1:p.Ser928=
XM_017011107.2:c.2604C>T	XP_016866596.1:p.Ser868=
XR_002956289.1:n.2867C>T
NM_001363725.2:c.453C>T	NP_001350654.1:p.Ser151=
NM_001371656.1:c.2991C>T	NP_001358585.1:p.Ser997=
NM_001374820.1:c.2991C>T	NP_001361749.1:p.Ser997=
NM_001374828.1:c.2952C>T MANE Select	NP_001361757.1:p.Ser984=
NM_017519.3:c.2952C>T	NP_059989.3:p.Ser984=