Canonical Allele Identifier: CA366227633

Gene: ARID1B

Linked Data

• dbSNP Id: rs940353111
• MyVariant Identifiers: chr6:g.157502191G>C (hg19) ; chr6:g.157181057G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181057G>C , CM000668.2:g.157181057G>C	GRCh38
NC_000006.11:g.157502191G>C , CM000668.1:g.157502191G>C	GRCh37
NC_000006.10:g.157543883G>C	NCBI36
NG_032093.1:g.408128G>C
NG_032093.2:g.408128G>C
NG_066624.1:g.410032G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3434G>C	ENSP00000055163.8:p.Arg1145Pro
ENST00000414678.8:c.3503G>C	ENSP00000412835.3:p.Arg1168Pro
ENST00000637015.2:c.3722G>C	ENSP00000489729.2:p.Arg1241Pro
ENST00000319584.11:c.1607G>C	ENSP00000313006.7:p.Arg536Pro
ENST00000346085.10:c.3473G>C	ENSP00000344546.5:p.Arg1158Pro
ENST00000350026.10:c.3185G>C	ENSP00000055163.7:p.Arg1062Pro
ENST00000414678.7:c.1751G>C	ENSP00000412835.2:p.Arg584Pro
ENST00000635849.1:c.914G>C	ENSP00000490948.1:p.Arg305Pro
ENST00000635957.1:c.548G>C	ENSP00000490385.1:p.Arg183Pro
ENST00000636930.2:c.3593G>C MANE Select	ENSP00000490491.2:p.Arg1198Pro
ENST00000636940.1:n.1590G>C
ENST00000637015.1:c.961G>C
ENST00000637568.1:c.875G>C
ENST00000637741.1:n.259G>C
ENST00000637810.1:c.935G>C	ENSP00000489636.1:p.Arg312Pro
ENST00000637904.1:c.1094G>C	ENSP00000490550.1:p.Arg365Pro
ENST00000647938.1:c.3224G>C	ENSP00000498155.1:p.Arg1075Pro
ENST00000319584.10:c.1610G>C	ENSP00000313006.6:p.Arg537Pro
ENST00000346085.9:c.3224G>C	ENSP00000344546.4:p.Arg1075Pro
ENST00000350026.9:c.3185G>C	ENSP00000055163.7:p.Arg1062Pro
ENST00000400790.3:c.386G>C	ENSP00000383596.3:p.Arg129Pro
ENST00000414678.6:c.1751G>C	ENSP00000412835.2:p.Arg584Pro
ENST00000478761.3:c.795G>C
NM_017519.2:c.3185G>C	NP_059989.2:p.Arg1062Pro
NM_020732.3:c.3224G>C	NP_065783.3:p.Arg1075Pro
XM_005267069.3:c.3344G>C	XP_005267126.2:p.Arg1115Pro
XM_011535984.1:c.2423G>C	XP_011534286.1:p.Arg808Pro
XM_011535985.1:c.2243G>C	XP_011534287.1:p.Arg748Pro
XM_011535986.1:c.2003G>C	XP_011534288.1:p.Arg668Pro
XM_011535987.1:c.1622G>C	XP_011534289.1:p.Arg541Pro
XM_011535988.1:c.485G>C	XP_011534290.1:p.Arg162Pro
NM_001346813.1:c.3344G>C	NP_001333742.1:p.Arg1115Pro
NM_001363725.1:c.1094G>C	NP_001350654.1:p.Arg365Pro
XM_011535984.2:c.3554G>C	XP_011534286.2:p.Arg1185Pro
XM_011535988.3:c.485G>C	XP_011534290.1:p.Arg162Pro
XM_017011103.2:c.3455G>C	XP_016866592.1:p.Arg1152Pro
XM_017011104.1:c.3425G>C	XP_016866593.1:p.Arg1142Pro
XM_017011105.2:c.3395G>C	XP_016866594.1:p.Arg1132Pro
XM_017011106.2:c.3266G>C	XP_016866595.1:p.Arg1089Pro
XM_017011107.2:c.3245G>C	XP_016866596.1:p.Arg1082Pro
XR_002956289.1:n.3637G>C
NM_001363725.2:c.1094G>C	NP_001350654.1:p.Arg365Pro
NM_001371656.1:c.3473G>C	NP_001358585.1:p.Arg1158Pro
NM_001374820.1:c.3473G>C	NP_001361749.1:p.Arg1158Pro
NM_001374828.1:c.3593G>C MANE Select	NP_001361757.1:p.Arg1198Pro
NM_017519.3:c.3434G>C	NP_059989.3:p.Arg1145Pro