Canonical Allele Identifier: CA366228205

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317574
• MyVariant Identifiers: chr6:g.157502262G>C (hg19) ; chr6:g.157181128G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181128G>C , CM000668.2:g.157181128G>C	GRCh38
NC_000006.11:g.157502262G>C , CM000668.1:g.157502262G>C	GRCh37
NC_000006.10:g.157543954G>C	NCBI36
NG_032093.1:g.408199G>C
NG_032093.2:g.408199G>C
NG_066624.1:g.410103G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3505G>C	ENSP00000055163.8:p.Asp1169His
ENST00000414678.8:c.3574G>C	ENSP00000412835.3:p.Asp1192His
ENST00000637015.2:c.3793G>C	ENSP00000489729.2:p.Asp1265His
ENST00000319584.11:c.1678G>C	ENSP00000313006.7:p.Asp560His
ENST00000346085.10:c.3544G>C	ENSP00000344546.5:p.Asp1182His
ENST00000350026.10:c.3256G>C	ENSP00000055163.7:p.Asp1086His
ENST00000414678.7:c.1822G>C	ENSP00000412835.2:p.Asp608His
ENST00000635849.1:c.985G>C	ENSP00000490948.1:p.Asp329His
ENST00000635957.1:c.619G>C	ENSP00000490385.1:p.Asp207His
ENST00000636930.2:c.3664G>C MANE Select	ENSP00000490491.2:p.Asp1222His
ENST00000636940.1:n.1661G>C
ENST00000637015.1:c.1032G>C
ENST00000637568.1:c.946G>C
ENST00000637741.1:n.330G>C
ENST00000637810.1:c.1006G>C	ENSP00000489636.1:p.Asp336His
ENST00000637904.1:c.1165G>C	ENSP00000490550.1:p.Asp389His
ENST00000647938.1:c.3295G>C	ENSP00000498155.1:p.Asp1099His
ENST00000319584.10:c.1681G>C	ENSP00000313006.6:p.Asp561His
ENST00000346085.9:c.3295G>C	ENSP00000344546.4:p.Asp1099His
ENST00000350026.9:c.3256G>C	ENSP00000055163.7:p.Asp1086His
ENST00000400790.3:c.457G>C	ENSP00000383596.3:p.Asp153His
ENST00000414678.6:c.1822G>C	ENSP00000412835.2:p.Asp608His
ENST00000478761.3:c.866G>C
NM_017519.2:c.3256G>C	NP_059989.2:p.Asp1086His
NM_020732.3:c.3295G>C	NP_065783.3:p.Asp1099His
XM_005267069.3:c.3415G>C	XP_005267126.2:p.Asp1139His
XM_011535984.1:c.2494G>C	XP_011534286.1:p.Asp832His
XM_011535985.1:c.2314G>C	XP_011534287.1:p.Asp772His
XM_011535986.1:c.2074G>C	XP_011534288.1:p.Asp692His
XM_011535987.1:c.1693G>C	XP_011534289.1:p.Asp565His
XM_011535988.1:c.556G>C	XP_011534290.1:p.Asp186His
NM_001346813.1:c.3415G>C	NP_001333742.1:p.Asp1139His
NM_001363725.1:c.1165G>C	NP_001350654.1:p.Asp389His
XM_011535984.2:c.3625G>C	XP_011534286.2:p.Asp1209His
XM_011535988.3:c.556G>C	XP_011534290.1:p.Asp186His
XM_017011103.2:c.3526G>C	XP_016866592.1:p.Asp1176His
XM_017011104.1:c.3496G>C	XP_016866593.1:p.Asp1166His
XM_017011105.2:c.3466G>C	XP_016866594.1:p.Asp1156His
XM_017011106.2:c.3337G>C	XP_016866595.1:p.Asp1113His
XM_017011107.2:c.3316G>C	XP_016866596.1:p.Asp1106His
XR_002956289.1:n.3708G>C
NM_001363725.2:c.1165G>C	NP_001350654.1:p.Asp389His
NM_001371656.1:c.3544G>C	NP_001358585.1:p.Asp1182His
NM_001374820.1:c.3544G>C	NP_001361749.1:p.Asp1182His
NM_001374828.1:c.3664G>C MANE Select	NP_001361757.1:p.Asp1222His
NM_017519.3:c.3505G>C	NP_059989.3:p.Asp1169His