Canonical Allele Identifier: CA366227871

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317256
• MyVariant Identifiers: chr6:g.157502213G>C (hg19) ; chr6:g.157181079G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181079G>C , CM000668.2:g.157181079G>C	GRCh38
NC_000006.11:g.157502213G>C , CM000668.1:g.157502213G>C	GRCh37
NC_000006.10:g.157543905G>C	NCBI36
NG_032093.1:g.408150G>C
NG_032093.2:g.408150G>C
NG_066624.1:g.410054G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3456G>C	ENSP00000055163.8:p.Glu1152Asp
ENST00000414678.8:c.3525G>C	ENSP00000412835.3:p.Glu1175Asp
ENST00000637015.2:c.3744G>C	ENSP00000489729.2:p.Glu1248Asp
ENST00000319584.11:c.1629G>C	ENSP00000313006.7:p.Glu543Asp
ENST00000346085.10:c.3495G>C	ENSP00000344546.5:p.Glu1165Asp
ENST00000350026.10:c.3207G>C	ENSP00000055163.7:p.Glu1069Asp
ENST00000414678.7:c.1773G>C	ENSP00000412835.2:p.Glu591Asp
ENST00000635849.1:c.936G>C	ENSP00000490948.1:p.Glu312Asp
ENST00000635957.1:c.570G>C	ENSP00000490385.1:p.Glu190Asp
ENST00000636930.2:c.3615G>C MANE Select	ENSP00000490491.2:p.Glu1205Asp
ENST00000636940.1:n.1612G>C
ENST00000637015.1:c.983G>C
ENST00000637568.1:c.897G>C
ENST00000637741.1:n.281G>C
ENST00000637810.1:c.957G>C	ENSP00000489636.1:p.Glu319Asp
ENST00000637904.1:c.1116G>C	ENSP00000490550.1:p.Glu372Asp
ENST00000647938.1:c.3246G>C	ENSP00000498155.1:p.Glu1082Asp
ENST00000319584.10:c.1632G>C	ENSP00000313006.6:p.Glu544Asp
ENST00000346085.9:c.3246G>C	ENSP00000344546.4:p.Glu1082Asp
ENST00000350026.9:c.3207G>C	ENSP00000055163.7:p.Glu1069Asp
ENST00000400790.3:c.408G>C	ENSP00000383596.3:p.Glu136Asp
ENST00000414678.6:c.1773G>C	ENSP00000412835.2:p.Glu591Asp
ENST00000478761.3:c.817G>C
NM_017519.2:c.3207G>C	NP_059989.2:p.Glu1069Asp
NM_020732.3:c.3246G>C	NP_065783.3:p.Glu1082Asp
XM_005267069.3:c.3366G>C	XP_005267126.2:p.Glu1122Asp
XM_011535984.1:c.2445G>C	XP_011534286.1:p.Glu815Asp
XM_011535985.1:c.2265G>C	XP_011534287.1:p.Glu755Asp
XM_011535986.1:c.2025G>C	XP_011534288.1:p.Glu675Asp
XM_011535987.1:c.1644G>C	XP_011534289.1:p.Glu548Asp
XM_011535988.1:c.507G>C	XP_011534290.1:p.Glu169Asp
NM_001346813.1:c.3366G>C	NP_001333742.1:p.Glu1122Asp
NM_001363725.1:c.1116G>C	NP_001350654.1:p.Glu372Asp
XM_011535984.2:c.3576G>C	XP_011534286.2:p.Glu1192Asp
XM_011535988.3:c.507G>C	XP_011534290.1:p.Glu169Asp
XM_017011103.2:c.3477G>C	XP_016866592.1:p.Glu1159Asp
XM_017011104.1:c.3447G>C	XP_016866593.1:p.Glu1149Asp
XM_017011105.2:c.3417G>C	XP_016866594.1:p.Glu1139Asp
XM_017011106.2:c.3288G>C	XP_016866595.1:p.Glu1096Asp
XM_017011107.2:c.3267G>C	XP_016866596.1:p.Glu1089Asp
XR_002956289.1:n.3659G>C
NM_001363725.2:c.1116G>C	NP_001350654.1:p.Glu372Asp
NM_001371656.1:c.3495G>C	NP_001358585.1:p.Glu1165Asp
NM_001374820.1:c.3495G>C	NP_001361749.1:p.Glu1165Asp
NM_001374828.1:c.3615G>C MANE Select	NP_001361757.1:p.Glu1205Asp
NM_017519.3:c.3456G>C	NP_059989.3:p.Glu1152Asp