Canonical Allele Identifier: CA150370074

Gene: ARID1B

Linked Data

• dbSNP Id: rs1033911742
• gnomAD v2: 6-157522138-T-C
• gnomAD v3: 6-157201004-T-C
• gnomAD v4: 6-157201004-T-C
• MyVariant Identifiers: chr6:g.157522138T>C (hg19) ; chr6:g.157201004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201004T>C , CM000668.2:g.157201004T>C	GRCh38
NC_000006.11:g.157522138T>C , CM000668.1:g.157522138T>C	GRCh37
NC_000006.10:g.157563830T>C	NCBI36
NG_032093.1:g.428075T>C
NG_032093.2:g.428075T>C
NG_066624.1:g.429979T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4620T>C	ENSP00000055163.8:p.Asp1540=
ENST00000414678.8:c.4689T>C	ENSP00000412835.3:p.Asp1563=
ENST00000637015.2:c.4908T>C	ENSP00000489729.2:p.Asp1636=
ENST00000346085.10:c.4659T>C	ENSP00000344546.5:p.Asp1553=
ENST00000350026.10:c.4371T>C	ENSP00000055163.7:p.Asp1457=
ENST00000414678.7:c.2937T>C	ENSP00000412835.2:p.Asp979=
ENST00000635849.1:c.2100T>C	ENSP00000490948.1:p.Asp700=
ENST00000635957.1:c.1731T>C	ENSP00000490385.1:p.Asp577=
ENST00000636227.1:n.3242T>C
ENST00000636254.1:n.699T>C
ENST00000636930.2:c.4779T>C MANE Select	ENSP00000490491.2:p.Asp1593=
ENST00000636940.1:n.2776T>C
ENST00000637015.1:c.2147T>C
ENST00000637568.1:c.2061T>C
ENST00000637741.1:n.1445T>C
ENST00000637810.1:c.2121T>C	ENSP00000489636.1:p.Asp707=
ENST00000637904.1:c.2280T>C	ENSP00000490550.1:p.Asp760=
ENST00000647938.1:c.4410T>C	ENSP00000498155.1:p.Asp1470=
ENST00000346085.9:c.4410T>C	ENSP00000344546.4:p.Asp1470=
ENST00000350026.9:c.4371T>C	ENSP00000055163.7:p.Asp1457=
ENST00000414678.6:c.2937T>C	ENSP00000412835.2:p.Asp979=
NM_017519.2:c.4371T>C	NP_059989.2:p.Asp1457=
NM_020732.3:c.4410T>C	NP_065783.3:p.Asp1470=
XM_005267069.3:c.4530T>C	XP_005267126.2:p.Asp1510=
XM_011535984.1:c.3609T>C	XP_011534286.1:p.Asp1203=
XM_011535985.1:c.3429T>C	XP_011534287.1:p.Asp1143=
XM_011535986.1:c.3189T>C	XP_011534288.1:p.Asp1063=
XM_011535987.1:c.2808T>C	XP_011534289.1:p.Asp936=
XM_011535988.1:c.1671T>C	XP_011534290.1:p.Asp557=
NM_001346813.1:c.4530T>C	NP_001333742.1:p.Asp1510=
NM_001363725.1:c.2280T>C	NP_001350654.1:p.Asp760=
XM_011535984.2:c.4740T>C	XP_011534286.2:p.Asp1580=
XM_011535988.3:c.1671T>C	XP_011534290.1:p.Asp557=
XM_017011103.2:c.4641T>C	XP_016866592.1:p.Asp1547=
XM_017011104.1:c.4611T>C	XP_016866593.1:p.Asp1537=
XM_017011105.2:c.4581T>C	XP_016866594.1:p.Asp1527=
XM_017011106.2:c.4452T>C	XP_016866595.1:p.Asp1484=
XM_017011107.2:c.4431T>C	XP_016866596.1:p.Asp1477=
XR_002956289.1:n.4726T>C
NM_001363725.2:c.2280T>C	NP_001350654.1:p.Asp760=
NM_001371656.1:c.4659T>C	NP_001358585.1:p.Asp1553=
NM_001374820.1:c.4659T>C	NP_001361749.1:p.Asp1553=
NM_001374828.1:c.4779T>C MANE Select	NP_001361757.1:p.Asp1593=
NM_017519.3:c.4620T>C	NP_059989.3:p.Asp1540=