Canonical Allele Identifier: CA452990108

Gene: ARID1B

Linked Data

• dbSNP Id: rs1789997991
• MyVariant Identifiers: chr6:g.157470047A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148913A>C , CM000668.2:g.157148913A>C	GRCh38
NC_000006.11:g.157470047A>C , CM000668.1:g.157470047A>C	GRCh37
NC_000006.10:g.157511739A>C	NCBI36
NG_032093.1:g.375984A>C
NG_032093.2:g.375984A>C
NG_066624.1:g.377888A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3051A>C	ENSP00000055163.8:p.Ala1017=
ENST00000414678.8:c.2961A>C	ENSP00000412835.3:p.Ala987=
ENST00000637015.2:c.3051A>C	ENSP00000489729.2:p.Ala1017=
ENST00000319584.11:c.1065A>C	ENSP00000313006.7:p.Ala355=
ENST00000346085.10:c.3090A>C	ENSP00000344546.5:p.Ala1030=
ENST00000350026.10:c.2802A>C	ENSP00000055163.7:p.Ala934=
ENST00000414678.7:c.1209A>C	ENSP00000412835.2:p.Ala403=
ENST00000452544.2:n.952A>C
ENST00000635849.1:c.372A>C	ENSP00000490948.1:p.Ala124=
ENST00000635957.1:c.6A>C	ENSP00000490385.1:p.Ala2=
ENST00000636426.1:n.185A>C
ENST00000636930.2:c.3051A>C MANE Select	ENSP00000490491.2:p.Ala1017=
ENST00000637015.1:c.290A>C
ENST00000637568.1:c.94A>C
ENST00000637810.1:c.552A>C	ENSP00000489636.1:p.Ala184=
ENST00000637904.1:c.552A>C	ENSP00000490550.1:p.Ala184=
ENST00000647938.1:c.2841A>C	ENSP00000498155.1:p.Ala947=
ENST00000674190.1:n.1800A>C
ENST00000319584.10:c.1068A>C	ENSP00000313006.6:p.Ala356=
ENST00000346085.9:c.2841A>C	ENSP00000344546.4:p.Ala947=
ENST00000350026.9:c.2802A>C	ENSP00000055163.7:p.Ala934=
ENST00000400790.3:c.3A>C	ENSP00000383596.3:p.Ala1=
ENST00000414678.6:c.1209A>C	ENSP00000412835.2:p.Ala403=
ENST00000452544.1:n.898A>C
ENST00000478761.3:c.124A>C
NM_017519.2:c.2802A>C	NP_059989.2:p.Ala934=
NM_020732.3:c.2841A>C	NP_065783.3:p.Ala947=
XM_005267069.3:c.2802A>C	XP_005267126.2:p.Ala934=
XM_011535984.1:c.1752A>C	XP_011534286.1:p.Ala584=
XM_011535985.1:c.1572A>C	XP_011534287.1:p.Ala524=
XM_011535986.1:c.1332A>C	XP_011534288.1:p.Ala444=
XM_011535987.1:c.951A>C	XP_011534289.1:p.Ala317=
XM_011535988.1:c.-20+15706A>C	XP_011534290.1:n.-20+15706A>C
NM_001346813.1:c.2802A>C	NP_001333742.1:p.Ala934=
NM_001363725.1:c.552A>C	NP_001350654.1:p.Ala184=
XM_011535984.2:c.2883A>C	XP_011534286.2:p.Ala961=
XM_011535988.3:c.-20+15706A>C	XP_011534290.1:n.-20+15706A>C
XM_017011103.2:c.2883A>C	XP_016866592.1:p.Ala961=
XM_017011104.1:c.2883A>C	XP_016866593.1:p.Ala961=
XM_017011105.2:c.2883A>C	XP_016866594.1:p.Ala961=
XM_017011106.2:c.2883A>C	XP_016866595.1:p.Ala961=
XM_017011107.2:c.2703A>C	XP_016866596.1:p.Ala901=
XR_002956289.1:n.2966A>C
NM_001363725.2:c.552A>C	NP_001350654.1:p.Ala184=
NM_001371656.1:c.3090A>C	NP_001358585.1:p.Ala1030=
NM_001374820.1:c.3090A>C	NP_001361749.1:p.Ala1030=
NM_001374828.1:c.3051A>C MANE Select	NP_001361757.1:p.Ala1017=
NM_017519.3:c.3051A>C	NP_059989.3:p.Ala1017=