Canonical Allele Identifier: CA452784737

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522492C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201358C>G , CM000668.2:g.157201358C>G	GRCh38
NC_000006.11:g.157522492C>G , CM000668.1:g.157522492C>G	GRCh37
NC_000006.10:g.157564184C>G	NCBI36
NG_032093.1:g.428429C>G
NG_032093.2:g.428429C>G
NG_066624.1:g.430333C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4974C>G	ENSP00000055163.8:p.Pro1658=
ENST00000414678.8:c.5043C>G	ENSP00000412835.3:p.Pro1681=
ENST00000637015.2:c.5262C>G	ENSP00000489729.2:p.Pro1754=
ENST00000346085.10:c.5013C>G	ENSP00000344546.5:p.Pro1671=
ENST00000350026.10:c.4725C>G	ENSP00000055163.7:p.Pro1575=
ENST00000414678.7:c.3291C>G	ENSP00000412835.2:p.Pro1097=
ENST00000635849.1:c.2454C>G	ENSP00000490948.1:p.Pro818=
ENST00000635957.1:c.2085C>G	ENSP00000490385.1:p.Pro695=
ENST00000636227.1:n.3596C>G
ENST00000636254.1:n.1053C>G
ENST00000636930.2:c.5133C>G MANE Select	ENSP00000490491.2:p.Pro1711=
ENST00000636940.1:n.3130C>G
ENST00000637015.1:c.2501C>G
ENST00000637568.1:c.2415C>G
ENST00000637741.1:n.1799C>G
ENST00000637810.1:c.2475C>G	ENSP00000489636.1:p.Pro825=
ENST00000637904.1:c.2634C>G	ENSP00000490550.1:p.Pro878=
ENST00000647938.1:c.4764C>G	ENSP00000498155.1:p.Pro1588=
ENST00000346085.9:c.4764C>G	ENSP00000344546.4:p.Pro1588=
ENST00000350026.9:c.4725C>G	ENSP00000055163.7:p.Pro1575=
ENST00000414678.6:c.3291C>G	ENSP00000412835.2:p.Pro1097=
NM_017519.2:c.4725C>G	NP_059989.2:p.Pro1575=
NM_020732.3:c.4764C>G	NP_065783.3:p.Pro1588=
XM_005267069.3:c.4884C>G	XP_005267126.2:p.Pro1628=
XM_011535984.1:c.3963C>G	XP_011534286.1:p.Pro1321=
XM_011535985.1:c.3783C>G	XP_011534287.1:p.Pro1261=
XM_011535986.1:c.3543C>G	XP_011534288.1:p.Pro1181=
XM_011535987.1:c.3162C>G	XP_011534289.1:p.Pro1054=
XM_011535988.1:c.2025C>G	XP_011534290.1:p.Pro675=
NM_001346813.1:c.4884C>G	NP_001333742.1:p.Pro1628=
NM_001363725.1:c.2634C>G	NP_001350654.1:p.Pro878=
XM_011535984.2:c.5094C>G	XP_011534286.2:p.Pro1698=
XM_011535988.3:c.2025C>G	XP_011534290.1:p.Pro675=
XM_017011103.2:c.4995C>G	XP_016866592.1:p.Pro1665=
XM_017011104.1:c.4965C>G	XP_016866593.1:p.Pro1655=
XM_017011105.2:c.4935C>G	XP_016866594.1:p.Pro1645=
XM_017011106.2:c.4806C>G	XP_016866595.1:p.Pro1602=
XM_017011107.2:c.4785C>G	XP_016866596.1:p.Pro1595=
XR_002956289.1:n.5080C>G
NM_001363725.2:c.2634C>G	NP_001350654.1:p.Pro878=
NM_001371656.1:c.5013C>G	NP_001358585.1:p.Pro1671=
NM_001374820.1:c.5013C>G	NP_001361749.1:p.Pro1671=
NM_001374828.1:c.5133C>G MANE Select	NP_001361757.1:p.Pro1711=
NM_017519.3:c.4974C>G	NP_059989.3:p.Pro1658=