Canonical Allele Identifier: CA366227715

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502203T>C (hg19) ; chr6:g.157181069T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181069T>C , CM000668.2:g.157181069T>C	GRCh38
NC_000006.11:g.157502203T>C , CM000668.1:g.157502203T>C	GRCh37
NC_000006.10:g.157543895T>C	NCBI36
NG_032093.1:g.408140T>C
NG_032093.2:g.408140T>C
NG_066624.1:g.410044T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3446T>C	ENSP00000055163.8:p.Phe1149Ser
ENST00000414678.8:c.3515T>C	ENSP00000412835.3:p.Phe1172Ser
ENST00000637015.2:c.3734T>C	ENSP00000489729.2:p.Phe1245Ser
ENST00000319584.11:c.1619T>C	ENSP00000313006.7:p.Phe540Ser
ENST00000346085.10:c.3485T>C	ENSP00000344546.5:p.Phe1162Ser
ENST00000350026.10:c.3197T>C	ENSP00000055163.7:p.Phe1066Ser
ENST00000414678.7:c.1763T>C	ENSP00000412835.2:p.Phe588Ser
ENST00000635849.1:c.926T>C	ENSP00000490948.1:p.Phe309Ser
ENST00000635957.1:c.560T>C	ENSP00000490385.1:p.Phe187Ser
ENST00000636930.2:c.3605T>C MANE Select	ENSP00000490491.2:p.Phe1202Ser
ENST00000636940.1:n.1602T>C
ENST00000637015.1:c.973T>C
ENST00000637568.1:c.887T>C
ENST00000637741.1:n.271T>C
ENST00000637810.1:c.947T>C	ENSP00000489636.1:p.Phe316Ser
ENST00000637904.1:c.1106T>C	ENSP00000490550.1:p.Phe369Ser
ENST00000647938.1:c.3236T>C	ENSP00000498155.1:p.Phe1079Ser
ENST00000319584.10:c.1622T>C	ENSP00000313006.6:p.Phe541Ser
ENST00000346085.9:c.3236T>C	ENSP00000344546.4:p.Phe1079Ser
ENST00000350026.9:c.3197T>C	ENSP00000055163.7:p.Phe1066Ser
ENST00000400790.3:c.398T>C	ENSP00000383596.3:p.Phe133Ser
ENST00000414678.6:c.1763T>C	ENSP00000412835.2:p.Phe588Ser
ENST00000478761.3:c.807T>C
NM_017519.2:c.3197T>C	NP_059989.2:p.Phe1066Ser
NM_020732.3:c.3236T>C	NP_065783.3:p.Phe1079Ser
XM_005267069.3:c.3356T>C	XP_005267126.2:p.Phe1119Ser
XM_011535984.1:c.2435T>C	XP_011534286.1:p.Phe812Ser
XM_011535985.1:c.2255T>C	XP_011534287.1:p.Phe752Ser
XM_011535986.1:c.2015T>C	XP_011534288.1:p.Phe672Ser
XM_011535987.1:c.1634T>C	XP_011534289.1:p.Phe545Ser
XM_011535988.1:c.497T>C	XP_011534290.1:p.Phe166Ser
NM_001346813.1:c.3356T>C	NP_001333742.1:p.Phe1119Ser
NM_001363725.1:c.1106T>C	NP_001350654.1:p.Phe369Ser
XM_011535984.2:c.3566T>C	XP_011534286.2:p.Phe1189Ser
XM_011535988.3:c.497T>C	XP_011534290.1:p.Phe166Ser
XM_017011103.2:c.3467T>C	XP_016866592.1:p.Phe1156Ser
XM_017011104.1:c.3437T>C	XP_016866593.1:p.Phe1146Ser
XM_017011105.2:c.3407T>C	XP_016866594.1:p.Phe1136Ser
XM_017011106.2:c.3278T>C	XP_016866595.1:p.Phe1093Ser
XM_017011107.2:c.3257T>C	XP_016866596.1:p.Phe1086Ser
XR_002956289.1:n.3649T>C
NM_001363725.2:c.1106T>C	NP_001350654.1:p.Phe369Ser
NM_001371656.1:c.3485T>C	NP_001358585.1:p.Phe1162Ser
NM_001374820.1:c.3485T>C	NP_001361749.1:p.Phe1162Ser
NM_001374828.1:c.3605T>C MANE Select	NP_001361757.1:p.Phe1202Ser
NM_017519.3:c.3446T>C	NP_059989.3:p.Phe1149Ser