Canonical Allele Identifier: CA366389214

Gene: ARID1B

Linked Data

• dbSNP Id: rs1156795543
• gnomAD v2: 6-157470039-G-C
• gnomAD v4: 6-157148905-G-C
• MyVariant Identifiers: chr6:g.157470039G>C (hg19) ; chr6:g.157148905G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148905G>C , CM000668.2:g.157148905G>C	GRCh38
NC_000006.11:g.157470039G>C , CM000668.1:g.157470039G>C	GRCh37
NC_000006.10:g.157511731G>C	NCBI36
NG_032093.1:g.375976G>C
NG_032093.2:g.375976G>C
NG_066624.1:g.377880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3043G>C	ENSP00000055163.8:p.Ala1015Pro
ENST00000414678.8:c.2953G>C	ENSP00000412835.3:p.Ala985Pro
ENST00000637015.2:c.3043G>C	ENSP00000489729.2:p.Ala1015Pro
ENST00000319584.11:c.1057G>C	ENSP00000313006.7:p.Ala353Pro
ENST00000346085.10:c.3082G>C	ENSP00000344546.5:p.Ala1028Pro
ENST00000350026.10:c.2794G>C	ENSP00000055163.7:p.Ala932Pro
ENST00000414678.7:c.1201G>C	ENSP00000412835.2:p.Ala401Pro
ENST00000452544.2:n.944G>C
ENST00000635849.1:c.364G>C	ENSP00000490948.1:p.Ala122Pro
ENST00000636426.1:n.177G>C
ENST00000636930.2:c.3043G>C MANE Select	ENSP00000490491.2:p.Ala1015Pro
ENST00000637015.1:c.282G>C
ENST00000637568.1:c.86G>C
ENST00000637810.1:c.544G>C	ENSP00000489636.1:p.Ala182Pro
ENST00000637904.1:c.544G>C	ENSP00000490550.1:p.Ala182Pro
ENST00000647938.1:c.2833G>C	ENSP00000498155.1:p.Ala945Pro
ENST00000674190.1:n.1792G>C
ENST00000319584.10:c.1060G>C	ENSP00000313006.6:p.Ala354Pro
ENST00000346085.9:c.2833G>C	ENSP00000344546.4:p.Ala945Pro
ENST00000350026.9:c.2794G>C	ENSP00000055163.7:p.Ala932Pro
ENST00000414678.6:c.1201G>C	ENSP00000412835.2:p.Ala401Pro
ENST00000452544.1:n.890G>C
ENST00000478761.3:c.116G>C
NM_017519.2:c.2794G>C	NP_059989.2:p.Ala932Pro
NM_020732.3:c.2833G>C	NP_065783.3:p.Ala945Pro
XM_005267069.3:c.2794G>C	XP_005267126.2:p.Ala932Pro
XM_011535984.1:c.1744G>C	XP_011534286.1:p.Ala582Pro
XM_011535985.1:c.1564G>C	XP_011534287.1:p.Ala522Pro
XM_011535986.1:c.1324G>C	XP_011534288.1:p.Ala442Pro
XM_011535987.1:c.943G>C	XP_011534289.1:p.Ala315Pro
XM_011535988.1:c.-20+15698G>C	XP_011534290.1:n.-20+15698G>C
NM_001346813.1:c.2794G>C	NP_001333742.1:p.Ala932Pro
NM_001363725.1:c.544G>C	NP_001350654.1:p.Ala182Pro
XM_011535984.2:c.2875G>C	XP_011534286.2:p.Ala959Pro
XM_011535988.3:c.-20+15698G>C	XP_011534290.1:n.-20+15698G>C
XM_017011103.2:c.2875G>C	XP_016866592.1:p.Ala959Pro
XM_017011104.1:c.2875G>C	XP_016866593.1:p.Ala959Pro
XM_017011105.2:c.2875G>C	XP_016866594.1:p.Ala959Pro
XM_017011106.2:c.2875G>C	XP_016866595.1:p.Ala959Pro
XM_017011107.2:c.2695G>C	XP_016866596.1:p.Ala899Pro
XR_002956289.1:n.2958G>C
NM_001363725.2:c.544G>C	NP_001350654.1:p.Ala182Pro
NM_001371656.1:c.3082G>C	NP_001358585.1:p.Ala1028Pro
NM_001374820.1:c.3082G>C	NP_001361749.1:p.Ala1028Pro
NM_001374828.1:c.3043G>C MANE Select	NP_001361757.1:p.Ala1015Pro
NM_017519.3:c.3043G>C	NP_059989.3:p.Ala1015Pro