Canonical Allele Identifier: CA366228038

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502229T>C (hg19) ; chr6:g.157181095T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181095T>C , CM000668.2:g.157181095T>C	GRCh38
NC_000006.11:g.157502229T>C , CM000668.1:g.157502229T>C	GRCh37
NC_000006.10:g.157543921T>C	NCBI36
NG_032093.1:g.408166T>C
NG_032093.2:g.408166T>C
NG_066624.1:g.410070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3472T>C	ENSP00000055163.8:p.Ser1158Pro
ENST00000414678.8:c.3541T>C	ENSP00000412835.3:p.Ser1181Pro
ENST00000637015.2:c.3760T>C	ENSP00000489729.2:p.Ser1254Pro
ENST00000319584.11:c.1645T>C	ENSP00000313006.7:p.Ser549Pro
ENST00000346085.10:c.3511T>C	ENSP00000344546.5:p.Ser1171Pro
ENST00000350026.10:c.3223T>C	ENSP00000055163.7:p.Ser1075Pro
ENST00000414678.7:c.1789T>C	ENSP00000412835.2:p.Ser597Pro
ENST00000635849.1:c.952T>C	ENSP00000490948.1:p.Ser318Pro
ENST00000635957.1:c.586T>C	ENSP00000490385.1:p.Ser196Pro
ENST00000636930.2:c.3631T>C MANE Select	ENSP00000490491.2:p.Ser1211Pro
ENST00000636940.1:n.1628T>C
ENST00000637015.1:c.999T>C
ENST00000637568.1:c.913T>C
ENST00000637741.1:n.297T>C
ENST00000637810.1:c.973T>C	ENSP00000489636.1:p.Ser325Pro
ENST00000637904.1:c.1132T>C	ENSP00000490550.1:p.Ser378Pro
ENST00000647938.1:c.3262T>C	ENSP00000498155.1:p.Ser1088Pro
ENST00000319584.10:c.1648T>C	ENSP00000313006.6:p.Ser550Pro
ENST00000346085.9:c.3262T>C	ENSP00000344546.4:p.Ser1088Pro
ENST00000350026.9:c.3223T>C	ENSP00000055163.7:p.Ser1075Pro
ENST00000400790.3:c.424T>C	ENSP00000383596.3:p.Ser142Pro
ENST00000414678.6:c.1789T>C	ENSP00000412835.2:p.Ser597Pro
ENST00000478761.3:c.833T>C
NM_017519.2:c.3223T>C	NP_059989.2:p.Ser1075Pro
NM_020732.3:c.3262T>C	NP_065783.3:p.Ser1088Pro
XM_005267069.3:c.3382T>C	XP_005267126.2:p.Ser1128Pro
XM_011535984.1:c.2461T>C	XP_011534286.1:p.Ser821Pro
XM_011535985.1:c.2281T>C	XP_011534287.1:p.Ser761Pro
XM_011535986.1:c.2041T>C	XP_011534288.1:p.Ser681Pro
XM_011535987.1:c.1660T>C	XP_011534289.1:p.Ser554Pro
XM_011535988.1:c.523T>C	XP_011534290.1:p.Ser175Pro
NM_001346813.1:c.3382T>C	NP_001333742.1:p.Ser1128Pro
NM_001363725.1:c.1132T>C	NP_001350654.1:p.Ser378Pro
XM_011535984.2:c.3592T>C	XP_011534286.2:p.Ser1198Pro
XM_011535988.3:c.523T>C	XP_011534290.1:p.Ser175Pro
XM_017011103.2:c.3493T>C	XP_016866592.1:p.Ser1165Pro
XM_017011104.1:c.3463T>C	XP_016866593.1:p.Ser1155Pro
XM_017011105.2:c.3433T>C	XP_016866594.1:p.Ser1145Pro
XM_017011106.2:c.3304T>C	XP_016866595.1:p.Ser1102Pro
XM_017011107.2:c.3283T>C	XP_016866596.1:p.Ser1095Pro
XR_002956289.1:n.3675T>C
NM_001363725.2:c.1132T>C	NP_001350654.1:p.Ser378Pro
NM_001371656.1:c.3511T>C	NP_001358585.1:p.Ser1171Pro
NM_001374820.1:c.3511T>C	NP_001361749.1:p.Ser1171Pro
NM_001374828.1:c.3631T>C MANE Select	NP_001361757.1:p.Ser1211Pro
NM_017519.3:c.3472T>C	NP_059989.3:p.Ser1158Pro