Canonical Allele Identifier: CA452990116

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470053G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148919G>C , CM000668.2:g.157148919G>C	GRCh38
NC_000006.11:g.157470053G>C , CM000668.1:g.157470053G>C	GRCh37
NC_000006.10:g.157511745G>C	NCBI36
NG_032093.1:g.375990G>C
NG_032093.2:g.375990G>C
NG_066624.1:g.377894G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3057G>C	ENSP00000055163.8:p.Val1019=
ENST00000414678.8:c.2967G>C	ENSP00000412835.3:p.Val989=
ENST00000637015.2:c.3057G>C	ENSP00000489729.2:p.Val1019=
ENST00000319584.11:c.1071G>C	ENSP00000313006.7:p.Val357=
ENST00000346085.10:c.3096G>C	ENSP00000344546.5:p.Val1032=
ENST00000350026.10:c.2808G>C	ENSP00000055163.7:p.Val936=
ENST00000414678.7:c.1215G>C	ENSP00000412835.2:p.Val405=
ENST00000452544.2:n.958G>C
ENST00000635849.1:c.378G>C	ENSP00000490948.1:p.Val126=
ENST00000635957.1:c.12G>C	ENSP00000490385.1:p.Val4=
ENST00000636426.1:n.191G>C
ENST00000636930.2:c.3057G>C MANE Select	ENSP00000490491.2:p.Val1019=
ENST00000637015.1:c.296G>C
ENST00000637568.1:c.100G>C
ENST00000637810.1:c.558G>C	ENSP00000489636.1:p.Val186=
ENST00000637904.1:c.558G>C	ENSP00000490550.1:p.Val186=
ENST00000647938.1:c.2847G>C	ENSP00000498155.1:p.Val949=
ENST00000674190.1:n.1806G>C
ENST00000319584.10:c.1074G>C	ENSP00000313006.6:p.Val358=
ENST00000346085.9:c.2847G>C	ENSP00000344546.4:p.Val949=
ENST00000350026.9:c.2808G>C	ENSP00000055163.7:p.Val936=
ENST00000400790.3:c.9G>C	ENSP00000383596.3:p.Val3=
ENST00000414678.6:c.1215G>C	ENSP00000412835.2:p.Val405=
ENST00000452544.1:n.904G>C
ENST00000478761.3:c.130G>C
NM_017519.2:c.2808G>C	NP_059989.2:p.Val936=
NM_020732.3:c.2847G>C	NP_065783.3:p.Val949=
XM_005267069.3:c.2808G>C	XP_005267126.2:p.Val936=
XM_011535984.1:c.1758G>C	XP_011534286.1:p.Val586=
XM_011535985.1:c.1578G>C	XP_011534287.1:p.Val526=
XM_011535986.1:c.1338G>C	XP_011534288.1:p.Val446=
XM_011535987.1:c.957G>C	XP_011534289.1:p.Val319=
XM_011535988.1:c.-20+15712G>C	XP_011534290.1:n.-20+15712G>C
NM_001346813.1:c.2808G>C	NP_001333742.1:p.Val936=
NM_001363725.1:c.558G>C	NP_001350654.1:p.Val186=
XM_011535984.2:c.2889G>C	XP_011534286.2:p.Val963=
XM_011535988.3:c.-20+15712G>C	XP_011534290.1:n.-20+15712G>C
XM_017011103.2:c.2889G>C	XP_016866592.1:p.Val963=
XM_017011104.1:c.2889G>C	XP_016866593.1:p.Val963=
XM_017011105.2:c.2889G>C	XP_016866594.1:p.Val963=
XM_017011106.2:c.2889G>C	XP_016866595.1:p.Val963=
XM_017011107.2:c.2709G>C	XP_016866596.1:p.Val903=
XR_002956289.1:n.2972G>C
NM_001363725.2:c.558G>C	NP_001350654.1:p.Val186=
NM_001371656.1:c.3096G>C	NP_001358585.1:p.Val1032=
NM_001374820.1:c.3096G>C	NP_001361749.1:p.Val1032=
NM_001374828.1:c.3057G>C MANE Select	NP_001361757.1:p.Val1019=
NM_017519.3:c.3057G>C	NP_059989.3:p.Val1019=