Canonical Allele Identifier: CA366242650

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201344-A-G
• MyVariant Identifiers: chr6:g.157522478A>G (hg19) ; chr6:g.157201344A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201344A>G , CM000668.2:g.157201344A>G	GRCh38
NC_000006.11:g.157522478A>G , CM000668.1:g.157522478A>G	GRCh37
NC_000006.10:g.157564170A>G	NCBI36
NG_032093.1:g.428415A>G
NG_032093.2:g.428415A>G
NG_066624.1:g.430319A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4960A>G	ENSP00000055163.8:p.Met1654Val
ENST00000414678.8:c.5029A>G	ENSP00000412835.3:p.Met1677Val
ENST00000637015.2:c.5248A>G	ENSP00000489729.2:p.Met1750Val
ENST00000346085.10:c.4999A>G	ENSP00000344546.5:p.Met1667Val
ENST00000350026.10:c.4711A>G	ENSP00000055163.7:p.Met1571Val
ENST00000414678.7:c.3277A>G	ENSP00000412835.2:p.Met1093Val
ENST00000635849.1:c.2440A>G	ENSP00000490948.1:p.Met814Val
ENST00000635957.1:c.2071A>G	ENSP00000490385.1:p.Met691Val
ENST00000636227.1:n.3582A>G
ENST00000636254.1:n.1039A>G
ENST00000636930.2:c.5119A>G MANE Select	ENSP00000490491.2:p.Met1707Val
ENST00000636940.1:n.3116A>G
ENST00000637015.1:c.2487A>G
ENST00000637568.1:c.2401A>G
ENST00000637741.1:n.1785A>G
ENST00000637810.1:c.2461A>G	ENSP00000489636.1:p.Met821Val
ENST00000637904.1:c.2620A>G	ENSP00000490550.1:p.Met874Val
ENST00000647938.1:c.4750A>G	ENSP00000498155.1:p.Met1584Val
ENST00000346085.9:c.4750A>G	ENSP00000344546.4:p.Met1584Val
ENST00000350026.9:c.4711A>G	ENSP00000055163.7:p.Met1571Val
ENST00000414678.6:c.3277A>G	ENSP00000412835.2:p.Met1093Val
NM_017519.2:c.4711A>G	NP_059989.2:p.Met1571Val
NM_020732.3:c.4750A>G	NP_065783.3:p.Met1584Val
XM_005267069.3:c.4870A>G	XP_005267126.2:p.Met1624Val
XM_011535984.1:c.3949A>G	XP_011534286.1:p.Met1317Val
XM_011535985.1:c.3769A>G	XP_011534287.1:p.Met1257Val
XM_011535986.1:c.3529A>G	XP_011534288.1:p.Met1177Val
XM_011535987.1:c.3148A>G	XP_011534289.1:p.Met1050Val
XM_011535988.1:c.2011A>G	XP_011534290.1:p.Met671Val
NM_001346813.1:c.4870A>G	NP_001333742.1:p.Met1624Val
NM_001363725.1:c.2620A>G	NP_001350654.1:p.Met874Val
XM_011535984.2:c.5080A>G	XP_011534286.2:p.Met1694Val
XM_011535988.3:c.2011A>G	XP_011534290.1:p.Met671Val
XM_017011103.2:c.4981A>G	XP_016866592.1:p.Met1661Val
XM_017011104.1:c.4951A>G	XP_016866593.1:p.Met1651Val
XM_017011105.2:c.4921A>G	XP_016866594.1:p.Met1641Val
XM_017011106.2:c.4792A>G	XP_016866595.1:p.Met1598Val
XM_017011107.2:c.4771A>G	XP_016866596.1:p.Met1591Val
XR_002956289.1:n.5066A>G
NM_001363725.2:c.2620A>G	NP_001350654.1:p.Met874Val
NM_001371656.1:c.4999A>G	NP_001358585.1:p.Met1667Val
NM_001374820.1:c.4999A>G	NP_001361749.1:p.Met1667Val
NM_001374828.1:c.5119A>G MANE Select	NP_001361757.1:p.Met1707Val
NM_017519.3:c.4960A>G	NP_059989.3:p.Met1654Val