Canonical Allele Identifier: CA366389024

Gene: ARID1B

Linked Data

• dbSNP Id: rs1789985355
• MyVariant Identifiers: chr6:g.157469952A>G (hg19) ; chr6:g.157148818A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148818A>G , CM000668.2:g.157148818A>G	GRCh38
NC_000006.11:g.157469952A>G , CM000668.1:g.157469952A>G	GRCh37
NC_000006.10:g.157511644A>G	NCBI36
NG_032093.1:g.375889A>G
NG_032093.2:g.375889A>G
NG_066624.1:g.377793A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2956A>G	ENSP00000055163.8:p.Met986Val
ENST00000414678.8:c.2866A>G	ENSP00000412835.3:p.Met956Val
ENST00000637015.2:c.2956A>G	ENSP00000489729.2:p.Met986Val
ENST00000319584.11:c.970A>G	ENSP00000313006.7:p.Met324Val
ENST00000346085.10:c.2995A>G	ENSP00000344546.5:p.Met999Val
ENST00000350026.10:c.2707A>G	ENSP00000055163.7:p.Met903Val
ENST00000414678.7:c.1114A>G	ENSP00000412835.2:p.Met372Val
ENST00000452544.2:n.857A>G
ENST00000635849.1:c.277A>G	ENSP00000490948.1:p.Met93Val
ENST00000636426.1:n.90A>G
ENST00000636930.2:c.2956A>G MANE Select	ENSP00000490491.2:p.Met986Val
ENST00000637015.1:c.195A>G
ENST00000637810.1:c.457A>G	ENSP00000489636.1:p.Met153Val
ENST00000637904.1:c.457A>G	ENSP00000490550.1:p.Met153Val
ENST00000647938.1:c.2746A>G	ENSP00000498155.1:p.Met916Val
ENST00000674190.1:n.1705A>G
ENST00000319584.10:c.973A>G	ENSP00000313006.6:p.Met325Val
ENST00000346085.9:c.2746A>G	ENSP00000344546.4:p.Met916Val
ENST00000350026.9:c.2707A>G	ENSP00000055163.7:p.Met903Val
ENST00000414678.6:c.1114A>G	ENSP00000412835.2:p.Met372Val
ENST00000452544.1:n.803A>G
ENST00000478761.3:c.29A>G
NM_017519.2:c.2707A>G	NP_059989.2:p.Met903Val
NM_020732.3:c.2746A>G	NP_065783.3:p.Met916Val
XM_005267069.3:c.2707A>G	XP_005267126.2:p.Met903Val
XM_011535984.1:c.1657A>G	XP_011534286.1:p.Met553Val
XM_011535985.1:c.1477A>G	XP_011534287.1:p.Met493Val
XM_011535986.1:c.1237A>G	XP_011534288.1:p.Met413Val
XM_011535987.1:c.856A>G	XP_011534289.1:p.Met286Val
XM_011535988.1:c.-20+15611A>G	XP_011534290.1:n.-20+15611A>G
NM_001346813.1:c.2707A>G	NP_001333742.1:p.Met903Val
NM_001363725.1:c.457A>G	NP_001350654.1:p.Met153Val
XM_011535984.2:c.2788A>G	XP_011534286.2:p.Met930Val
XM_011535988.3:c.-20+15611A>G	XP_011534290.1:n.-20+15611A>G
XM_017011103.2:c.2788A>G	XP_016866592.1:p.Met930Val
XM_017011104.1:c.2788A>G	XP_016866593.1:p.Met930Val
XM_017011105.2:c.2788A>G	XP_016866594.1:p.Met930Val
XM_017011106.2:c.2788A>G	XP_016866595.1:p.Met930Val
XM_017011107.2:c.2608A>G	XP_016866596.1:p.Met870Val
XR_002956289.1:n.2871A>G
NM_001363725.2:c.457A>G	NP_001350654.1:p.Met153Val
NM_001371656.1:c.2995A>G	NP_001358585.1:p.Met999Val
NM_001374820.1:c.2995A>G	NP_001361749.1:p.Met999Val
NM_001374828.1:c.2956A>G MANE Select	NP_001361757.1:p.Met986Val
NM_017519.3:c.2956A>G	NP_059989.3:p.Met986Val