Canonical Allele Identifier: CA366234247

Gene: ARID1B

Linked Data

• dbSNP Id: rs748391706
• gnomAD v4: 6-157189757-G-C
• MyVariant Identifiers: chr6:g.157510891G>C (hg19) ; chr6:g.157189757G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189757G>C , CM000668.2:g.157189757G>C	GRCh38
NC_000006.11:g.157510891G>C , CM000668.1:g.157510891G>C	GRCh37
NC_000006.10:g.157552583G>C	NCBI36
NG_032093.1:g.416828G>C
NG_032093.2:g.416828G>C
NG_066624.1:g.418732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3876G>C	ENSP00000055163.8:p.Gln1292His
ENST00000414678.8:c.3945G>C	ENSP00000412835.3:p.Gln1315His
ENST00000637015.2:c.4164G>C	ENSP00000489729.2:p.Gln1388His
ENST00000346085.10:c.3915G>C	ENSP00000344546.5:p.Gln1305His
ENST00000350026.10:c.3627G>C	ENSP00000055163.7:p.Gln1209His
ENST00000414678.7:c.2193G>C	ENSP00000412835.2:p.Gln731His
ENST00000635849.1:c.1356G>C	ENSP00000490948.1:p.Gln452His
ENST00000635957.1:c.990G>C	ENSP00000490385.1:p.Gln330His
ENST00000636930.2:c.4035G>C MANE Select	ENSP00000490491.2:p.Gln1345His
ENST00000636940.1:n.2032G>C
ENST00000637015.1:c.1403G>C
ENST00000637568.1:c.1317G>C
ENST00000637741.1:n.701G>C
ENST00000637810.1:c.1377G>C	ENSP00000489636.1:p.Gln459His
ENST00000637904.1:c.1536G>C	ENSP00000490550.1:p.Gln512His
ENST00000647938.1:c.3666G>C	ENSP00000498155.1:p.Gln1222His
ENST00000346085.9:c.3666G>C	ENSP00000344546.4:p.Gln1222His
ENST00000350026.9:c.3627G>C	ENSP00000055163.7:p.Gln1209His
ENST00000414678.6:c.2193G>C	ENSP00000412835.2:p.Gln731His
NM_017519.2:c.3627G>C	NP_059989.2:p.Gln1209His
NM_020732.3:c.3666G>C	NP_065783.3:p.Gln1222His
XM_005267069.3:c.3786G>C	XP_005267126.2:p.Gln1262His
XM_011535984.1:c.2865G>C	XP_011534286.1:p.Gln955His
XM_011535985.1:c.2685G>C	XP_011534287.1:p.Gln895His
XM_011535986.1:c.2445G>C	XP_011534288.1:p.Gln815His
XM_011535987.1:c.2064G>C	XP_011534289.1:p.Gln688His
XM_011535988.1:c.927G>C	XP_011534290.1:p.Gln309His
NM_001346813.1:c.3786G>C	NP_001333742.1:p.Gln1262His
NM_001363725.1:c.1536G>C	NP_001350654.1:p.Gln512His
XM_011535984.2:c.3996G>C	XP_011534286.2:p.Gln1332His
XM_011535988.3:c.927G>C	XP_011534290.1:p.Gln309His
XM_017011103.2:c.3897G>C	XP_016866592.1:p.Gln1299His
XM_017011104.1:c.3867G>C	XP_016866593.1:p.Gln1289His
XM_017011105.2:c.3837G>C	XP_016866594.1:p.Gln1279His
XM_017011106.2:c.3708G>C	XP_016866595.1:p.Gln1236His
XM_017011107.2:c.3687G>C	XP_016866596.1:p.Gln1229His
XR_002956289.1:n.4079G>C
NM_001363725.2:c.1536G>C	NP_001350654.1:p.Gln512His
NM_001371656.1:c.3915G>C	NP_001358585.1:p.Gln1305His
NM_001374820.1:c.3915G>C	NP_001361749.1:p.Gln1305His
NM_001374828.1:c.4035G>C MANE Select	NP_001361757.1:p.Gln1345His
NM_017519.3:c.3876G>C	NP_059989.3:p.Gln1292His