Canonical Allele Identifier: CA366227366

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128316905
• MyVariant Identifiers: chr6:g.157502161A>G (hg19) ; chr6:g.157181027A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181027A>G , CM000668.2:g.157181027A>G	GRCh38
NC_000006.11:g.157502161A>G , CM000668.1:g.157502161A>G	GRCh37
NC_000006.10:g.157543853A>G	NCBI36
NG_032093.1:g.408098A>G
NG_032093.2:g.408098A>G
NG_066624.1:g.410002A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3404A>G	ENSP00000055163.8:p.Asn1135Ser
ENST00000414678.8:c.3473A>G	ENSP00000412835.3:p.Asn1158Ser
ENST00000637015.2:c.3692A>G	ENSP00000489729.2:p.Asn1231Ser
ENST00000319584.11:c.1577A>G	ENSP00000313006.7:p.Asn526Ser
ENST00000346085.10:c.3443A>G	ENSP00000344546.5:p.Asn1148Ser
ENST00000350026.10:c.3155A>G	ENSP00000055163.7:p.Asn1052Ser
ENST00000414678.7:c.1721A>G	ENSP00000412835.2:p.Asn574Ser
ENST00000635849.1:c.884A>G	ENSP00000490948.1:p.Asn295Ser
ENST00000635957.1:c.518A>G	ENSP00000490385.1:p.Asn173Ser
ENST00000636930.2:c.3563A>G MANE Select	ENSP00000490491.2:p.Asn1188Ser
ENST00000636940.1:n.1560A>G
ENST00000637015.1:c.931A>G
ENST00000637568.1:c.845A>G
ENST00000637741.1:n.229A>G
ENST00000637810.1:c.905A>G	ENSP00000489636.1:p.Asn302Ser
ENST00000637904.1:c.1064A>G	ENSP00000490550.1:p.Asn355Ser
ENST00000647938.1:c.3194A>G	ENSP00000498155.1:p.Asn1065Ser
ENST00000319584.10:c.1580A>G	ENSP00000313006.6:p.Asn527Ser
ENST00000346085.9:c.3194A>G	ENSP00000344546.4:p.Asn1065Ser
ENST00000350026.9:c.3155A>G	ENSP00000055163.7:p.Asn1052Ser
ENST00000400790.3:c.356A>G	ENSP00000383596.3:p.Asn119Ser
ENST00000414678.6:c.1721A>G	ENSP00000412835.2:p.Asn574Ser
ENST00000478761.3:c.765A>G
NM_017519.2:c.3155A>G	NP_059989.2:p.Asn1052Ser
NM_020732.3:c.3194A>G	NP_065783.3:p.Asn1065Ser
XM_005267069.3:c.3314A>G	XP_005267126.2:p.Asn1105Ser
XM_011535984.1:c.2393A>G	XP_011534286.1:p.Asn798Ser
XM_011535985.1:c.2213A>G	XP_011534287.1:p.Asn738Ser
XM_011535986.1:c.1973A>G	XP_011534288.1:p.Asn658Ser
XM_011535987.1:c.1592A>G	XP_011534289.1:p.Asn531Ser
XM_011535988.1:c.455A>G	XP_011534290.1:p.Asn152Ser
NM_001346813.1:c.3314A>G	NP_001333742.1:p.Asn1105Ser
NM_001363725.1:c.1064A>G	NP_001350654.1:p.Asn355Ser
XM_011535984.2:c.3524A>G	XP_011534286.2:p.Asn1175Ser
XM_011535988.3:c.455A>G	XP_011534290.1:p.Asn152Ser
XM_017011103.2:c.3425A>G	XP_016866592.1:p.Asn1142Ser
XM_017011104.1:c.3395A>G	XP_016866593.1:p.Asn1132Ser
XM_017011105.2:c.3365A>G	XP_016866594.1:p.Asn1122Ser
XM_017011106.2:c.3236A>G	XP_016866595.1:p.Asn1079Ser
XM_017011107.2:c.3215A>G	XP_016866596.1:p.Asn1072Ser
XR_002956289.1:n.3607A>G
NM_001363725.2:c.1064A>G	NP_001350654.1:p.Asn355Ser
NM_001371656.1:c.3443A>G	NP_001358585.1:p.Asn1148Ser
NM_001374820.1:c.3443A>G	NP_001361749.1:p.Asn1148Ser
NM_001374828.1:c.3563A>G MANE Select	NP_001361757.1:p.Asn1188Ser
NM_017519.3:c.3404A>G	NP_059989.3:p.Asn1135Ser