Canonical Allele Identifier: CA366242542

Gene: ARID1B

Linked Data

• dbSNP Id: rs139214813
• MyVariant Identifiers: chr6:g.157522460A>T (hg19) ; chr6:g.157201326A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201326A>T , CM000668.2:g.157201326A>T	GRCh38
NC_000006.11:g.157522460A>T , CM000668.1:g.157522460A>T	GRCh37
NC_000006.10:g.157564152A>T	NCBI36
NG_032093.1:g.428397A>T
NG_032093.2:g.428397A>T
NG_066624.1:g.430301A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4942A>T	ENSP00000055163.8:p.Met1648Leu
ENST00000414678.8:c.5011A>T	ENSP00000412835.3:p.Met1671Leu
ENST00000637015.2:c.5230A>T	ENSP00000489729.2:p.Met1744Leu
ENST00000346085.10:c.4981A>T	ENSP00000344546.5:p.Met1661Leu
ENST00000350026.10:c.4693A>T	ENSP00000055163.7:p.Met1565Leu
ENST00000414678.7:c.3259A>T	ENSP00000412835.2:p.Met1087Leu
ENST00000635849.1:c.2422A>T	ENSP00000490948.1:p.Met808Leu
ENST00000635957.1:c.2053A>T	ENSP00000490385.1:p.Met685Leu
ENST00000636227.1:n.3564A>T
ENST00000636254.1:n.1021A>T
ENST00000636930.2:c.5101A>T MANE Select	ENSP00000490491.2:p.Met1701Leu
ENST00000636940.1:n.3098A>T
ENST00000637015.1:c.2469A>T
ENST00000637568.1:c.2383A>T
ENST00000637741.1:n.1767A>T
ENST00000637810.1:c.2443A>T	ENSP00000489636.1:p.Met815Leu
ENST00000637904.1:c.2602A>T	ENSP00000490550.1:p.Met868Leu
ENST00000647938.1:c.4732A>T	ENSP00000498155.1:p.Met1578Leu
ENST00000346085.9:c.4732A>T	ENSP00000344546.4:p.Met1578Leu
ENST00000350026.9:c.4693A>T	ENSP00000055163.7:p.Met1565Leu
ENST00000414678.6:c.3259A>T	ENSP00000412835.2:p.Met1087Leu
NM_017519.2:c.4693A>T	NP_059989.2:p.Met1565Leu
NM_020732.3:c.4732A>T	NP_065783.3:p.Met1578Leu
XM_005267069.3:c.4852A>T	XP_005267126.2:p.Met1618Leu
XM_011535984.1:c.3931A>T	XP_011534286.1:p.Met1311Leu
XM_011535985.1:c.3751A>T	XP_011534287.1:p.Met1251Leu
XM_011535986.1:c.3511A>T	XP_011534288.1:p.Met1171Leu
XM_011535987.1:c.3130A>T	XP_011534289.1:p.Met1044Leu
XM_011535988.1:c.1993A>T	XP_011534290.1:p.Met665Leu
NM_001346813.1:c.4852A>T	NP_001333742.1:p.Met1618Leu
NM_001363725.1:c.2602A>T	NP_001350654.1:p.Met868Leu
XM_011535984.2:c.5062A>T	XP_011534286.2:p.Met1688Leu
XM_011535988.3:c.1993A>T	XP_011534290.1:p.Met665Leu
XM_017011103.2:c.4963A>T	XP_016866592.1:p.Met1655Leu
XM_017011104.1:c.4933A>T	XP_016866593.1:p.Met1645Leu
XM_017011105.2:c.4903A>T	XP_016866594.1:p.Met1635Leu
XM_017011106.2:c.4774A>T	XP_016866595.1:p.Met1592Leu
XM_017011107.2:c.4753A>T	XP_016866596.1:p.Met1585Leu
XR_002956289.1:n.5048A>T
NM_001363725.2:c.2602A>T	NP_001350654.1:p.Met868Leu
NM_001371656.1:c.4981A>T	NP_001358585.1:p.Met1661Leu
NM_001374820.1:c.4981A>T	NP_001361749.1:p.Met1661Leu
NM_001374828.1:c.5101A>T MANE Select	NP_001361757.1:p.Met1701Leu
NM_017519.3:c.4942A>T	NP_059989.3:p.Met1648Leu