Canonical Allele Identifier: CA4067175

Gene: ARID1B

Linked Data

• dbSNP Id: rs531418921
• ExAC: 6:157470009 A / G
• gnomAD v2: 6-157470009-A-G
• gnomAD v3: 6-157148875-A-G
• gnomAD v4: 6-157148875-A-G
• MyVariant Identifiers: chr6:g.157470009A>G (hg19) ; chr6:g.157148875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148875A>G , CM000668.2:g.157148875A>G	GRCh38
NC_000006.11:g.157470009A>G , CM000668.1:g.157470009A>G	GRCh37
NC_000006.10:g.157511701A>G	NCBI36
NG_032093.1:g.375946A>G
NG_032093.2:g.375946A>G
NG_066624.1:g.377850A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3013A>G	ENSP00000055163.8:p.Met1005Val
ENST00000414678.8:c.2923A>G	ENSP00000412835.3:p.Met975Val
ENST00000637015.2:c.3013A>G	ENSP00000489729.2:p.Met1005Val
ENST00000319584.11:c.1027A>G	ENSP00000313006.7:p.Met343Val
ENST00000346085.10:c.3052A>G	ENSP00000344546.5:p.Met1018Val
ENST00000350026.10:c.2764A>G	ENSP00000055163.7:p.Met922Val
ENST00000414678.7:c.1171A>G	ENSP00000412835.2:p.Met391Val
ENST00000452544.2:n.914A>G
ENST00000635849.1:c.334A>G	ENSP00000490948.1:p.Met112Val
ENST00000636426.1:n.147A>G
ENST00000636930.2:c.3013A>G MANE Select	ENSP00000490491.2:p.Met1005Val
ENST00000637015.1:c.252A>G
ENST00000637568.1:c.56A>G
ENST00000637810.1:c.514A>G	ENSP00000489636.1:p.Met172Val
ENST00000637904.1:c.514A>G	ENSP00000490550.1:p.Met172Val
ENST00000647938.1:c.2803A>G	ENSP00000498155.1:p.Met935Val
ENST00000674190.1:n.1762A>G
ENST00000319584.10:c.1030A>G	ENSP00000313006.6:p.Met344Val
ENST00000346085.9:c.2803A>G	ENSP00000344546.4:p.Met935Val
ENST00000350026.9:c.2764A>G	ENSP00000055163.7:p.Met922Val
ENST00000414678.6:c.1171A>G	ENSP00000412835.2:p.Met391Val
ENST00000452544.1:n.860A>G
ENST00000478761.3:c.86A>G
NM_017519.2:c.2764A>G	NP_059989.2:p.Met922Val
NM_020732.3:c.2803A>G	NP_065783.3:p.Met935Val
XM_005267069.3:c.2764A>G	XP_005267126.2:p.Met922Val
XM_011535984.1:c.1714A>G	XP_011534286.1:p.Met572Val
XM_011535985.1:c.1534A>G	XP_011534287.1:p.Met512Val
XM_011535986.1:c.1294A>G	XP_011534288.1:p.Met432Val
XM_011535987.1:c.913A>G	XP_011534289.1:p.Met305Val
XM_011535988.1:c.-20+15668A>G	XP_011534290.1:n.-20+15668A>G
NM_001346813.1:c.2764A>G	NP_001333742.1:p.Met922Val
NM_001363725.1:c.514A>G	NP_001350654.1:p.Met172Val
XM_011535984.2:c.2845A>G	XP_011534286.2:p.Met949Val
XM_011535988.3:c.-20+15668A>G	XP_011534290.1:n.-20+15668A>G
XM_017011103.2:c.2845A>G	XP_016866592.1:p.Met949Val
XM_017011104.1:c.2845A>G	XP_016866593.1:p.Met949Val
XM_017011105.2:c.2845A>G	XP_016866594.1:p.Met949Val
XM_017011106.2:c.2845A>G	XP_016866595.1:p.Met949Val
XM_017011107.2:c.2665A>G	XP_016866596.1:p.Met889Val
XR_002956289.1:n.2928A>G
NM_001363725.2:c.514A>G	NP_001350654.1:p.Met172Val
NM_001371656.1:c.3052A>G	NP_001358585.1:p.Met1018Val
NM_001374820.1:c.3052A>G	NP_001361749.1:p.Met1018Val
NM_001374828.1:c.3013A>G MANE Select	NP_001361757.1:p.Met1005Val
NM_017519.3:c.3013A>G	NP_059989.3:p.Met1005Val