Canonical Allele Identifier: CA366234374

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189772-A-C
• MyVariant Identifiers: chr6:g.157510906A>C (hg19) ; chr6:g.157189772A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189772A>C , CM000668.2:g.157189772A>C	GRCh38
NC_000006.11:g.157510906A>C , CM000668.1:g.157510906A>C	GRCh37
NC_000006.10:g.157552598A>C	NCBI36
NG_032093.1:g.416843A>C
NG_032093.2:g.416843A>C
NG_066624.1:g.418747A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3891A>C	ENSP00000055163.8:p.Gln1297His
ENST00000414678.8:c.3960A>C	ENSP00000412835.3:p.Gln1320His
ENST00000637015.2:c.4179A>C	ENSP00000489729.2:p.Gln1393His
ENST00000346085.10:c.3930A>C	ENSP00000344546.5:p.Gln1310His
ENST00000350026.10:c.3642A>C	ENSP00000055163.7:p.Gln1214His
ENST00000414678.7:c.2208A>C	ENSP00000412835.2:p.Gln736His
ENST00000635849.1:c.1371A>C	ENSP00000490948.1:p.Gln457His
ENST00000635957.1:c.1005A>C	ENSP00000490385.1:p.Gln335His
ENST00000636930.2:c.4050A>C MANE Select	ENSP00000490491.2:p.Gln1350His
ENST00000636940.1:n.2047A>C
ENST00000637015.1:c.1418A>C
ENST00000637568.1:c.1332A>C
ENST00000637741.1:n.716A>C
ENST00000637810.1:c.1392A>C	ENSP00000489636.1:p.Gln464His
ENST00000637904.1:c.1551A>C	ENSP00000490550.1:p.Gln517His
ENST00000647938.1:c.3681A>C	ENSP00000498155.1:p.Gln1227His
ENST00000346085.9:c.3681A>C	ENSP00000344546.4:p.Gln1227His
ENST00000350026.9:c.3642A>C	ENSP00000055163.7:p.Gln1214His
ENST00000414678.6:c.2208A>C	ENSP00000412835.2:p.Gln736His
NM_017519.2:c.3642A>C	NP_059989.2:p.Gln1214His
NM_020732.3:c.3681A>C	NP_065783.3:p.Gln1227His
XM_005267069.3:c.3801A>C	XP_005267126.2:p.Gln1267His
XM_011535984.1:c.2880A>C	XP_011534286.1:p.Gln960His
XM_011535985.1:c.2700A>C	XP_011534287.1:p.Gln900His
XM_011535986.1:c.2460A>C	XP_011534288.1:p.Gln820His
XM_011535987.1:c.2079A>C	XP_011534289.1:p.Gln693His
XM_011535988.1:c.942A>C	XP_011534290.1:p.Gln314His
NM_001346813.1:c.3801A>C	NP_001333742.1:p.Gln1267His
NM_001363725.1:c.1551A>C	NP_001350654.1:p.Gln517His
XM_011535984.2:c.4011A>C	XP_011534286.2:p.Gln1337His
XM_011535988.3:c.942A>C	XP_011534290.1:p.Gln314His
XM_017011103.2:c.3912A>C	XP_016866592.1:p.Gln1304His
XM_017011104.1:c.3882A>C	XP_016866593.1:p.Gln1294His
XM_017011105.2:c.3852A>C	XP_016866594.1:p.Gln1284His
XM_017011106.2:c.3723A>C	XP_016866595.1:p.Gln1241His
XM_017011107.2:c.3702A>C	XP_016866596.1:p.Gln1234His
XR_002956289.1:n.4094A>C
NM_001363725.2:c.1551A>C	NP_001350654.1:p.Gln517His
NM_001371656.1:c.3930A>C	NP_001358585.1:p.Gln1310His
NM_001374820.1:c.3930A>C	NP_001361749.1:p.Gln1310His
NM_001374828.1:c.4050A>C MANE Select	NP_001361757.1:p.Gln1350His
NM_017519.3:c.3891A>C	NP_059989.3:p.Gln1297His