Canonical Allele Identifier: CA366389132

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470001G>C (hg19) ; chr6:g.157148867G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148867G>C , CM000668.2:g.157148867G>C	GRCh38
NC_000006.11:g.157470001G>C , CM000668.1:g.157470001G>C	GRCh37
NC_000006.10:g.157511693G>C	NCBI36
NG_032093.1:g.375938G>C
NG_032093.2:g.375938G>C
NG_066624.1:g.377842G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3005G>C	ENSP00000055163.8:p.Gly1002Ala
ENST00000414678.8:c.2915G>C	ENSP00000412835.3:p.Gly972Ala
ENST00000637015.2:c.3005G>C	ENSP00000489729.2:p.Gly1002Ala
ENST00000319584.11:c.1019G>C	ENSP00000313006.7:p.Gly340Ala
ENST00000346085.10:c.3044G>C	ENSP00000344546.5:p.Gly1015Ala
ENST00000350026.10:c.2756G>C	ENSP00000055163.7:p.Gly919Ala
ENST00000414678.7:c.1163G>C	ENSP00000412835.2:p.Gly388Ala
ENST00000452544.2:n.906G>C
ENST00000635849.1:c.326G>C	ENSP00000490948.1:p.Gly109Ala
ENST00000636426.1:n.139G>C
ENST00000636930.2:c.3005G>C MANE Select	ENSP00000490491.2:p.Gly1002Ala
ENST00000637015.1:c.244G>C
ENST00000637568.1:c.48G>C
ENST00000637810.1:c.506G>C	ENSP00000489636.1:p.Gly169Ala
ENST00000637904.1:c.506G>C	ENSP00000490550.1:p.Gly169Ala
ENST00000647938.1:c.2795G>C	ENSP00000498155.1:p.Gly932Ala
ENST00000674190.1:n.1754G>C
ENST00000319584.10:c.1022G>C	ENSP00000313006.6:p.Gly341Ala
ENST00000346085.9:c.2795G>C	ENSP00000344546.4:p.Gly932Ala
ENST00000350026.9:c.2756G>C	ENSP00000055163.7:p.Gly919Ala
ENST00000414678.6:c.1163G>C	ENSP00000412835.2:p.Gly388Ala
ENST00000452544.1:n.852G>C
ENST00000478761.3:c.78G>C
NM_017519.2:c.2756G>C	NP_059989.2:p.Gly919Ala
NM_020732.3:c.2795G>C	NP_065783.3:p.Gly932Ala
XM_005267069.3:c.2756G>C	XP_005267126.2:p.Gly919Ala
XM_011535984.1:c.1706G>C	XP_011534286.1:p.Gly569Ala
XM_011535985.1:c.1526G>C	XP_011534287.1:p.Gly509Ala
XM_011535986.1:c.1286G>C	XP_011534288.1:p.Gly429Ala
XM_011535987.1:c.905G>C	XP_011534289.1:p.Gly302Ala
XM_011535988.1:c.-20+15660G>C	XP_011534290.1:n.-20+15660G>C
NM_001346813.1:c.2756G>C	NP_001333742.1:p.Gly919Ala
NM_001363725.1:c.506G>C	NP_001350654.1:p.Gly169Ala
XM_011535984.2:c.2837G>C	XP_011534286.2:p.Gly946Ala
XM_011535988.3:c.-20+15660G>C	XP_011534290.1:n.-20+15660G>C
XM_017011103.2:c.2837G>C	XP_016866592.1:p.Gly946Ala
XM_017011104.1:c.2837G>C	XP_016866593.1:p.Gly946Ala
XM_017011105.2:c.2837G>C	XP_016866594.1:p.Gly946Ala
XM_017011106.2:c.2837G>C	XP_016866595.1:p.Gly946Ala
XM_017011107.2:c.2657G>C	XP_016866596.1:p.Gly886Ala
XR_002956289.1:n.2920G>C
NM_001363725.2:c.506G>C	NP_001350654.1:p.Gly169Ala
NM_001371656.1:c.3044G>C	NP_001358585.1:p.Gly1015Ala
NM_001374820.1:c.3044G>C	NP_001361749.1:p.Gly1015Ala
NM_001374828.1:c.3005G>C MANE Select	NP_001361757.1:p.Gly1002Ala
NM_017519.3:c.3005G>C	NP_059989.3:p.Gly1002Ala