Canonical Allele Identifier: CA366388784

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469842A>C (hg19) ; chr6:g.157148708A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148708A>C , CM000668.2:g.157148708A>C	GRCh38
NC_000006.11:g.157469842A>C , CM000668.1:g.157469842A>C	GRCh37
NC_000006.10:g.157511534A>C	NCBI36
NG_032093.1:g.375779A>C
NG_032093.2:g.375779A>C
NG_066624.1:g.377683A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2846A>C	ENSP00000055163.8:p.Asn949Thr
ENST00000414678.8:c.2756A>C	ENSP00000412835.3:p.Asn919Thr
ENST00000637015.2:c.2846A>C	ENSP00000489729.2:p.Asn949Thr
ENST00000319584.11:c.860A>C	ENSP00000313006.7:p.Asn287Thr
ENST00000346085.10:c.2885A>C	ENSP00000344546.5:p.Asn962Thr
ENST00000350026.10:c.2597A>C	ENSP00000055163.7:p.Asn866Thr
ENST00000414678.7:c.1004A>C	ENSP00000412835.2:p.Asn335Thr
ENST00000452544.2:n.747A>C
ENST00000635849.1:c.167A>C	ENSP00000490948.1:p.Asn56Thr
ENST00000636930.2:c.2846A>C MANE Select	ENSP00000490491.2:p.Asn949Thr
ENST00000637015.1:c.85A>C
ENST00000637810.1:c.347A>C	ENSP00000489636.1:p.Asn116Thr
ENST00000637904.1:c.347A>C	ENSP00000490550.1:p.Asn116Thr
ENST00000647938.1:c.2636A>C	ENSP00000498155.1:p.Asn879Thr
ENST00000674190.1:n.1595A>C
ENST00000319584.10:c.863A>C	ENSP00000313006.6:p.Asn288Thr
ENST00000346085.9:c.2636A>C	ENSP00000344546.4:p.Asn879Thr
ENST00000350026.9:c.2597A>C	ENSP00000055163.7:p.Asn866Thr
ENST00000414678.6:c.1004A>C	ENSP00000412835.2:p.Asn335Thr
ENST00000452544.1:n.693A>C
NM_017519.2:c.2597A>C	NP_059989.2:p.Asn866Thr
NM_020732.3:c.2636A>C	NP_065783.3:p.Asn879Thr
XM_005267069.3:c.2597A>C	XP_005267126.2:p.Asn866Thr
XM_011535984.1:c.1547A>C	XP_011534286.1:p.Asn516Thr
XM_011535985.1:c.1367A>C	XP_011534287.1:p.Asn456Thr
XM_011535986.1:c.1127A>C	XP_011534288.1:p.Asn376Thr
XM_011535987.1:c.746A>C	XP_011534289.1:p.Asn249Thr
XM_011535988.1:c.-20+15501A>C	XP_011534290.1:n.-20+15501A>C
NM_001346813.1:c.2597A>C	NP_001333742.1:p.Asn866Thr
NM_001363725.1:c.347A>C	NP_001350654.1:p.Asn116Thr
XM_011535984.2:c.2678A>C	XP_011534286.2:p.Asn893Thr
XM_011535988.3:c.-20+15501A>C	XP_011534290.1:n.-20+15501A>C
XM_017011103.2:c.2678A>C	XP_016866592.1:p.Asn893Thr
XM_017011104.1:c.2678A>C	XP_016866593.1:p.Asn893Thr
XM_017011105.2:c.2678A>C	XP_016866594.1:p.Asn893Thr
XM_017011106.2:c.2678A>C	XP_016866595.1:p.Asn893Thr
XM_017011107.2:c.2498A>C	XP_016866596.1:p.Asn833Thr
XR_002956289.1:n.2761A>C
NM_001363725.2:c.347A>C	NP_001350654.1:p.Asn116Thr
NM_001371656.1:c.2885A>C	NP_001358585.1:p.Asn962Thr
NM_001374820.1:c.2885A>C	NP_001361749.1:p.Asn962Thr
NM_001374828.1:c.2846A>C MANE Select	NP_001361757.1:p.Asn949Thr
NM_017519.3:c.2846A>C	NP_059989.3:p.Asn949Thr