Canonical Allele Identifier: CA366389288

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470075G>T (hg19) ; chr6:g.157148941G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148941G>T , CM000668.2:g.157148941G>T	GRCh38
NC_000006.11:g.157470075G>T , CM000668.1:g.157470075G>T	GRCh37
NC_000006.10:g.157511767G>T	NCBI36
NG_032093.1:g.376012G>T
NG_032093.2:g.376012G>T
NG_066624.1:g.377916G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3079G>T	ENSP00000055163.8:p.Ala1027Ser
ENST00000414678.8:c.2989G>T	ENSP00000412835.3:p.Ala997Ser
ENST00000637015.2:c.3079G>T	ENSP00000489729.2:p.Ala1027Ser
ENST00000319584.11:c.1093G>T	ENSP00000313006.7:p.Ala365Ser
ENST00000346085.10:c.3118G>T	ENSP00000344546.5:p.Ala1040Ser
ENST00000350026.10:c.2830G>T	ENSP00000055163.7:p.Ala944Ser
ENST00000414678.7:c.1237G>T	ENSP00000412835.2:p.Ala413Ser
ENST00000452544.2:n.980G>T
ENST00000635849.1:c.400G>T	ENSP00000490948.1:p.Ala134Ser
ENST00000635957.1:c.34G>T	ENSP00000490385.1:p.Ala12Ser
ENST00000636426.1:n.213G>T
ENST00000636930.2:c.3079G>T MANE Select	ENSP00000490491.2:p.Ala1027Ser
ENST00000637015.1:c.318G>T
ENST00000637568.1:c.122G>T
ENST00000637810.1:c.580G>T	ENSP00000489636.1:p.Ala194Ser
ENST00000637904.1:c.580G>T	ENSP00000490550.1:p.Ala194Ser
ENST00000647938.1:c.2869G>T	ENSP00000498155.1:p.Ala957Ser
ENST00000674190.1:n.1828G>T
ENST00000319584.10:c.1096G>T	ENSP00000313006.6:p.Ala366Ser
ENST00000346085.9:c.2869G>T	ENSP00000344546.4:p.Ala957Ser
ENST00000350026.9:c.2830G>T	ENSP00000055163.7:p.Ala944Ser
ENST00000400790.3:c.31G>T	ENSP00000383596.3:p.Ala11Ser
ENST00000414678.6:c.1237G>T	ENSP00000412835.2:p.Ala413Ser
ENST00000452544.1:n.926G>T
ENST00000478761.3:c.152G>T
NM_017519.2:c.2830G>T	NP_059989.2:p.Ala944Ser
NM_020732.3:c.2869G>T	NP_065783.3:p.Ala957Ser
XM_005267069.3:c.2830G>T	XP_005267126.2:p.Ala944Ser
XM_011535984.1:c.1780G>T	XP_011534286.1:p.Ala594Ser
XM_011535985.1:c.1600G>T	XP_011534287.1:p.Ala534Ser
XM_011535986.1:c.1360G>T	XP_011534288.1:p.Ala454Ser
XM_011535987.1:c.979G>T	XP_011534289.1:p.Ala327Ser
XM_011535988.1:c.-20+15734G>T	XP_011534290.1:n.-20+15734G>T
NM_001346813.1:c.2830G>T	NP_001333742.1:p.Ala944Ser
NM_001363725.1:c.580G>T	NP_001350654.1:p.Ala194Ser
XM_011535984.2:c.2911G>T	XP_011534286.2:p.Ala971Ser
XM_011535988.3:c.-20+15734G>T	XP_011534290.1:n.-20+15734G>T
XM_017011103.2:c.2911G>T	XP_016866592.1:p.Ala971Ser
XM_017011104.1:c.2911G>T	XP_016866593.1:p.Ala971Ser
XM_017011105.2:c.2911G>T	XP_016866594.1:p.Ala971Ser
XM_017011106.2:c.2911G>T	XP_016866595.1:p.Ala971Ser
XM_017011107.2:c.2731G>T	XP_016866596.1:p.Ala911Ser
XR_002956289.1:n.2994G>T
NM_001363725.2:c.580G>T	NP_001350654.1:p.Ala194Ser
NM_001371656.1:c.3118G>T	NP_001358585.1:p.Ala1040Ser
NM_001374820.1:c.3118G>T	NP_001361749.1:p.Ala1040Ser
NM_001374828.1:c.3079G>T MANE Select	NP_001361757.1:p.Ala1027Ser
NM_017519.3:c.3079G>T	NP_059989.3:p.Ala1027Ser