Canonical Allele Identifier: CA366233995

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510778A>T (hg19) ; chr6:g.157189644A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189644A>T , CM000668.2:g.157189644A>T	GRCh38
NC_000006.11:g.157510778A>T , CM000668.1:g.157510778A>T	GRCh37
NC_000006.10:g.157552470A>T	NCBI36
NG_032093.1:g.416715A>T
NG_032093.2:g.416715A>T
NG_066624.1:g.418619A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3763A>T	ENSP00000055163.8:p.Asn1255Tyr
ENST00000414678.8:c.3832A>T	ENSP00000412835.3:p.Asn1278Tyr
ENST00000637015.2:c.4051A>T	ENSP00000489729.2:p.Asn1351Tyr
ENST00000346085.10:c.3802A>T	ENSP00000344546.5:p.Asn1268Tyr
ENST00000350026.10:c.3514A>T	ENSP00000055163.7:p.Asn1172Tyr
ENST00000414678.7:c.2080A>T	ENSP00000412835.2:p.Asn694Tyr
ENST00000635849.1:c.1243A>T	ENSP00000490948.1:p.Asn415Tyr
ENST00000635957.1:c.877A>T	ENSP00000490385.1:p.Asn293Tyr
ENST00000636930.2:c.3922A>T MANE Select	ENSP00000490491.2:p.Asn1308Tyr
ENST00000636940.1:n.1919A>T
ENST00000637015.1:c.1290A>T
ENST00000637568.1:c.1204A>T
ENST00000637741.1:n.588A>T
ENST00000637810.1:c.1264A>T	ENSP00000489636.1:p.Asn422Tyr
ENST00000637904.1:c.1423A>T	ENSP00000490550.1:p.Asn475Tyr
ENST00000647938.1:c.3553A>T	ENSP00000498155.1:p.Asn1185Tyr
ENST00000346085.9:c.3553A>T	ENSP00000344546.4:p.Asn1185Tyr
ENST00000350026.9:c.3514A>T	ENSP00000055163.7:p.Asn1172Tyr
ENST00000414678.6:c.2080A>T	ENSP00000412835.2:p.Asn694Tyr
NM_017519.2:c.3514A>T	NP_059989.2:p.Asn1172Tyr
NM_020732.3:c.3553A>T	NP_065783.3:p.Asn1185Tyr
XM_005267069.3:c.3673A>T	XP_005267126.2:p.Asn1225Tyr
XM_011535984.1:c.2752A>T	XP_011534286.1:p.Asn918Tyr
XM_011535985.1:c.2572A>T	XP_011534287.1:p.Asn858Tyr
XM_011535986.1:c.2332A>T	XP_011534288.1:p.Asn778Tyr
XM_011535987.1:c.1951A>T	XP_011534289.1:p.Asn651Tyr
XM_011535988.1:c.814A>T	XP_011534290.1:p.Asn272Tyr
NM_001346813.1:c.3673A>T	NP_001333742.1:p.Asn1225Tyr
NM_001363725.1:c.1423A>T	NP_001350654.1:p.Asn475Tyr
XM_011535984.2:c.3883A>T	XP_011534286.2:p.Asn1295Tyr
XM_011535988.3:c.814A>T	XP_011534290.1:p.Asn272Tyr
XM_017011103.2:c.3784A>T	XP_016866592.1:p.Asn1262Tyr
XM_017011104.1:c.3754A>T	XP_016866593.1:p.Asn1252Tyr
XM_017011105.2:c.3724A>T	XP_016866594.1:p.Asn1242Tyr
XM_017011106.2:c.3595A>T	XP_016866595.1:p.Asn1199Tyr
XM_017011107.2:c.3574A>T	XP_016866596.1:p.Asn1192Tyr
XR_002956289.1:n.3966A>T
NM_001363725.2:c.1423A>T	NP_001350654.1:p.Asn475Tyr
NM_001371656.1:c.3802A>T	NP_001358585.1:p.Asn1268Tyr
NM_001374820.1:c.3802A>T	NP_001361749.1:p.Asn1268Tyr
NM_001374828.1:c.3922A>T MANE Select	NP_001361757.1:p.Asn1308Tyr
NM_017519.3:c.3763A>T	NP_059989.3:p.Asn1255Tyr