Canonical Allele Identifier: CA366388643

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128633947
• MyVariant Identifiers: chr6:g.157469778G>C (hg19) ; chr6:g.157148644G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148644G>C , CM000668.2:g.157148644G>C	GRCh38
NC_000006.11:g.157469778G>C , CM000668.1:g.157469778G>C	GRCh37
NC_000006.10:g.157511470G>C	NCBI36
NG_032093.1:g.375715G>C
NG_032093.2:g.375715G>C
NG_066624.1:g.377619G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2782G>C	ENSP00000055163.8:p.Ala928Pro
ENST00000414678.8:c.2692G>C	ENSP00000412835.3:p.Ala898Pro
ENST00000637015.2:c.2782G>C	ENSP00000489729.2:p.Ala928Pro
ENST00000319584.11:c.796G>C	ENSP00000313006.7:p.Ala266Pro
ENST00000346085.10:c.2821G>C	ENSP00000344546.5:p.Ala941Pro
ENST00000350026.10:c.2533G>C	ENSP00000055163.7:p.Ala845Pro
ENST00000414678.7:c.940G>C	ENSP00000412835.2:p.Ala314Pro
ENST00000452544.2:n.683G>C
ENST00000635849.1:c.103G>C	ENSP00000490948.1:p.Ala35Pro
ENST00000636930.2:c.2782G>C MANE Select	ENSP00000490491.2:p.Ala928Pro
ENST00000637015.1:c.21G>C
ENST00000637810.1:c.283G>C	ENSP00000489636.1:p.Ala95Pro
ENST00000637904.1:c.283G>C	ENSP00000490550.1:p.Ala95Pro
ENST00000647938.1:c.2572G>C	ENSP00000498155.1:p.Ala858Pro
ENST00000674190.1:n.1531G>C
ENST00000319584.10:c.799G>C	ENSP00000313006.6:p.Ala267Pro
ENST00000346085.9:c.2572G>C	ENSP00000344546.4:p.Ala858Pro
ENST00000350026.9:c.2533G>C	ENSP00000055163.7:p.Ala845Pro
ENST00000414678.6:c.940G>C	ENSP00000412835.2:p.Ala314Pro
ENST00000452544.1:n.629G>C
NM_017519.2:c.2533G>C	NP_059989.2:p.Ala845Pro
NM_020732.3:c.2572G>C	NP_065783.3:p.Ala858Pro
XM_005267069.3:c.2533G>C	XP_005267126.2:p.Ala845Pro
XM_011535984.1:c.1483G>C	XP_011534286.1:p.Ala495Pro
XM_011535985.1:c.1303G>C	XP_011534287.1:p.Ala435Pro
XM_011535986.1:c.1063G>C	XP_011534288.1:p.Ala355Pro
XM_011535987.1:c.682G>C	XP_011534289.1:p.Ala228Pro
XM_011535988.1:c.-20+15437G>C	XP_011534290.1:n.-20+15437G>C
NM_001346813.1:c.2533G>C	NP_001333742.1:p.Ala845Pro
NM_001363725.1:c.283G>C	NP_001350654.1:p.Ala95Pro
XM_011535984.2:c.2614G>C	XP_011534286.2:p.Ala872Pro
XM_011535988.3:c.-20+15437G>C	XP_011534290.1:n.-20+15437G>C
XM_017011103.2:c.2614G>C	XP_016866592.1:p.Ala872Pro
XM_017011104.1:c.2614G>C	XP_016866593.1:p.Ala872Pro
XM_017011105.2:c.2614G>C	XP_016866594.1:p.Ala872Pro
XM_017011106.2:c.2614G>C	XP_016866595.1:p.Ala872Pro
XM_017011107.2:c.2434G>C	XP_016866596.1:p.Ala812Pro
XR_002956289.1:n.2697G>C
NM_001363725.2:c.283G>C	NP_001350654.1:p.Ala95Pro
NM_001371656.1:c.2821G>C	NP_001358585.1:p.Ala941Pro
NM_001374820.1:c.2821G>C	NP_001361749.1:p.Ala941Pro
NM_001374828.1:c.2782G>C MANE Select	NP_001361757.1:p.Ala928Pro
NM_017519.3:c.2782G>C	NP_059989.3:p.Ala928Pro