Canonical Allele Identifier: CA366227367

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502161A>C (hg19) ; chr6:g.157181027A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3404A>C	ENSP00000055163.8:p.Asn1135Thr
ENST00000414678.8:c.3473A>C	ENSP00000412835.3:p.Asn1158Thr
ENST00000637015.2:c.3692A>C	ENSP00000489729.2:p.Asn1231Thr
ENST00000319584.11:c.1577A>C	ENSP00000313006.7:p.Asn526Thr
ENST00000346085.10:c.3443A>C	ENSP00000344546.5:p.Asn1148Thr
ENST00000350026.10:c.3155A>C	ENSP00000055163.7:p.Asn1052Thr
ENST00000414678.7:c.1721A>C	ENSP00000412835.2:p.Asn574Thr
ENST00000635849.1:c.884A>C	ENSP00000490948.1:p.Asn295Thr
ENST00000635957.1:c.518A>C	ENSP00000490385.1:p.Asn173Thr
ENST00000636930.2:c.3563A>C MANE Select	ENSP00000490491.2:p.Asn1188Thr
ENST00000636940.1:n.1560A>C
ENST00000637015.1:c.931A>C
ENST00000637568.1:c.845A>C
ENST00000637741.1:n.229A>C
ENST00000637810.1:c.905A>C	ENSP00000489636.1:p.Asn302Thr
ENST00000637904.1:c.1064A>C	ENSP00000490550.1:p.Asn355Thr
ENST00000647938.1:c.3194A>C	ENSP00000498155.1:p.Asn1065Thr
ENST00000319584.10:c.1580A>C	ENSP00000313006.6:p.Asn527Thr
ENST00000346085.9:c.3194A>C	ENSP00000344546.4:p.Asn1065Thr
ENST00000350026.9:c.3155A>C	ENSP00000055163.7:p.Asn1052Thr
ENST00000400790.3:c.356A>C	ENSP00000383596.3:p.Asn119Thr
ENST00000414678.6:c.1721A>C	ENSP00000412835.2:p.Asn574Thr
ENST00000478761.3:c.765A>C
NM_017519.2:c.3155A>C	NP_059989.2:p.Asn1052Thr
NM_020732.3:c.3194A>C	NP_065783.3:p.Asn1065Thr
XM_005267069.3:c.3314A>C	XP_005267126.2:p.Asn1105Thr
XM_011535984.1:c.2393A>C	XP_011534286.1:p.Asn798Thr
XM_011535985.1:c.2213A>C	XP_011534287.1:p.Asn738Thr
XM_011535986.1:c.1973A>C	XP_011534288.1:p.Asn658Thr
XM_011535987.1:c.1592A>C	XP_011534289.1:p.Asn531Thr
XM_011535988.1:c.455A>C	XP_011534290.1:p.Asn152Thr
NM_001346813.1:c.3314A>C	NP_001333742.1:p.Asn1105Thr
NM_001363725.1:c.1064A>C	NP_001350654.1:p.Asn355Thr
XM_011535984.2:c.3524A>C	XP_011534286.2:p.Asn1175Thr
XM_011535988.3:c.455A>C	XP_011534290.1:p.Asn152Thr
XM_017011103.2:c.3425A>C	XP_016866592.1:p.Asn1142Thr
XM_017011104.1:c.3395A>C	XP_016866593.1:p.Asn1132Thr
XM_017011105.2:c.3365A>C	XP_016866594.1:p.Asn1122Thr
XM_017011106.2:c.3236A>C	XP_016866595.1:p.Asn1079Thr
XM_017011107.2:c.3215A>C	XP_016866596.1:p.Asn1072Thr
XR_002956289.1:n.3607A>C
NM_001363725.2:c.1064A>C	NP_001350654.1:p.Asn355Thr
NM_001371656.1:c.3443A>C	NP_001358585.1:p.Asn1148Thr
NM_001374820.1:c.3443A>C	NP_001361749.1:p.Asn1148Thr
NM_001374828.1:c.3563A>C MANE Select	NP_001361757.1:p.Asn1188Thr
NM_017519.3:c.3404A>C	NP_059989.3:p.Asn1135Thr