Canonical Allele Identifier: CA366230338

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128325263
• MyVariant Identifiers: chr6:g.157505451G>C (hg19) ; chr6:g.157184317G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184317G>C , CM000668.2:g.157184317G>C	GRCh38
NC_000006.11:g.157505451G>C , CM000668.1:g.157505451G>C	GRCh37
NC_000006.10:g.157547143G>C	NCBI36
NG_032093.1:g.411388G>C
NG_032093.2:g.411388G>C
NG_066624.1:g.413292G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3642G>C	ENSP00000055163.8:p.Gln1214His
ENST00000414678.8:c.3711G>C	ENSP00000412835.3:p.Gln1237His
ENST00000637015.2:c.3930G>C	ENSP00000489729.2:p.Gln1310His
ENST00000319584.11:c.1815G>C	ENSP00000313006.7:p.Gln605His
ENST00000346085.10:c.3681G>C	ENSP00000344546.5:p.Gln1227His
ENST00000350026.10:c.3393G>C	ENSP00000055163.7:p.Gln1131His
ENST00000414678.7:c.1959G>C	ENSP00000412835.2:p.Gln653His
ENST00000635849.1:c.1122G>C	ENSP00000490948.1:p.Gln374His
ENST00000635957.1:c.756G>C	ENSP00000490385.1:p.Gln252His
ENST00000636930.2:c.3801G>C MANE Select	ENSP00000490491.2:p.Gln1267His
ENST00000636940.1:n.1798G>C
ENST00000637015.1:c.1169G>C
ENST00000637568.1:c.1083G>C
ENST00000637741.1:n.467G>C
ENST00000637810.1:c.1143G>C	ENSP00000489636.1:p.Gln381His
ENST00000637904.1:c.1302G>C	ENSP00000490550.1:p.Gln434His
ENST00000647938.1:c.3432G>C	ENSP00000498155.1:p.Gln1144His
ENST00000319584.10:c.1818G>C	ENSP00000313006.6:p.Gln606His
ENST00000346085.9:c.3432G>C	ENSP00000344546.4:p.Gln1144His
ENST00000350026.9:c.3393G>C	ENSP00000055163.7:p.Gln1131His
ENST00000400790.3:c.594G>C	ENSP00000383596.3:p.Gln198His
ENST00000414678.6:c.1959G>C	ENSP00000412835.2:p.Gln653His
NM_017519.2:c.3393G>C	NP_059989.2:p.Gln1131His
NM_020732.3:c.3432G>C	NP_065783.3:p.Gln1144His
XM_005267069.3:c.3552G>C	XP_005267126.2:p.Gln1184His
XM_011535984.1:c.2631G>C	XP_011534286.1:p.Gln877His
XM_011535985.1:c.2451G>C	XP_011534287.1:p.Gln817His
XM_011535986.1:c.2211G>C	XP_011534288.1:p.Gln737His
XM_011535987.1:c.1830G>C	XP_011534289.1:p.Gln610His
XM_011535988.1:c.693G>C	XP_011534290.1:p.Gln231His
NM_001346813.1:c.3552G>C	NP_001333742.1:p.Gln1184His
NM_001363725.1:c.1302G>C	NP_001350654.1:p.Gln434His
XM_011535984.2:c.3762G>C	XP_011534286.2:p.Gln1254His
XM_011535988.3:c.693G>C	XP_011534290.1:p.Gln231His
XM_017011103.2:c.3663G>C	XP_016866592.1:p.Gln1221His
XM_017011104.1:c.3633G>C	XP_016866593.1:p.Gln1211His
XM_017011105.2:c.3603G>C	XP_016866594.1:p.Gln1201His
XM_017011106.2:c.3474G>C	XP_016866595.1:p.Gln1158His
XM_017011107.2:c.3453G>C	XP_016866596.1:p.Gln1151His
XR_002956289.1:n.3845G>C
NM_001363725.2:c.1302G>C	NP_001350654.1:p.Gln434His
NM_001371656.1:c.3681G>C	NP_001358585.1:p.Gln1227His
NM_001374820.1:c.3681G>C	NP_001361749.1:p.Gln1227His
NM_001374828.1:c.3801G>C MANE Select	NP_001361757.1:p.Gln1267His
NM_017519.3:c.3642G>C	NP_059989.3:p.Gln1214His