Canonical Allele Identifier: CA4067178

Gene: ARID1B

Linked Data

• dbSNP Id: rs756655213
• ExAC: 6:157470025 G / C
• gnomAD v2: 6-157470025-G-C
• MyVariant Identifiers: chr6:g.157470025G>C (hg19) ; chr6:g.157148891G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148891G>C , CM000668.2:g.157148891G>C	GRCh38
NC_000006.11:g.157470025G>C , CM000668.1:g.157470025G>C	GRCh37
NC_000006.10:g.157511717G>C	NCBI36
NG_032093.1:g.375962G>C
NG_032093.2:g.375962G>C
NG_066624.1:g.377866G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3029G>C	ENSP00000055163.8:p.Arg1010Pro
ENST00000414678.8:c.2939G>C	ENSP00000412835.3:p.Arg980Pro
ENST00000637015.2:c.3029G>C	ENSP00000489729.2:p.Arg1010Pro
ENST00000319584.11:c.1043G>C	ENSP00000313006.7:p.Arg348Pro
ENST00000346085.10:c.3068G>C	ENSP00000344546.5:p.Arg1023Pro
ENST00000350026.10:c.2780G>C	ENSP00000055163.7:p.Arg927Pro
ENST00000414678.7:c.1187G>C	ENSP00000412835.2:p.Arg396Pro
ENST00000452544.2:n.930G>C
ENST00000635849.1:c.350G>C	ENSP00000490948.1:p.Arg117Pro
ENST00000636426.1:n.163G>C
ENST00000636930.2:c.3029G>C MANE Select	ENSP00000490491.2:p.Arg1010Pro
ENST00000637015.1:c.268G>C
ENST00000637568.1:c.72G>C
ENST00000637810.1:c.530G>C	ENSP00000489636.1:p.Arg177Pro
ENST00000637904.1:c.530G>C	ENSP00000490550.1:p.Arg177Pro
ENST00000647938.1:c.2819G>C	ENSP00000498155.1:p.Arg940Pro
ENST00000674190.1:n.1778G>C
ENST00000319584.10:c.1046G>C	ENSP00000313006.6:p.Arg349Pro
ENST00000346085.9:c.2819G>C	ENSP00000344546.4:p.Arg940Pro
ENST00000350026.9:c.2780G>C	ENSP00000055163.7:p.Arg927Pro
ENST00000414678.6:c.1187G>C	ENSP00000412835.2:p.Arg396Pro
ENST00000452544.1:n.876G>C
ENST00000478761.3:c.102G>C
NM_017519.2:c.2780G>C	NP_059989.2:p.Arg927Pro
NM_020732.3:c.2819G>C	NP_065783.3:p.Arg940Pro
XM_005267069.3:c.2780G>C	XP_005267126.2:p.Arg927Pro
XM_011535984.1:c.1730G>C	XP_011534286.1:p.Arg577Pro
XM_011535985.1:c.1550G>C	XP_011534287.1:p.Arg517Pro
XM_011535986.1:c.1310G>C	XP_011534288.1:p.Arg437Pro
XM_011535987.1:c.929G>C	XP_011534289.1:p.Arg310Pro
XM_011535988.1:c.-20+15684G>C	XP_011534290.1:n.-20+15684G>C
NM_001346813.1:c.2780G>C	NP_001333742.1:p.Arg927Pro
NM_001363725.1:c.530G>C	NP_001350654.1:p.Arg177Pro
XM_011535984.2:c.2861G>C	XP_011534286.2:p.Arg954Pro
XM_011535988.3:c.-20+15684G>C	XP_011534290.1:n.-20+15684G>C
XM_017011103.2:c.2861G>C	XP_016866592.1:p.Arg954Pro
XM_017011104.1:c.2861G>C	XP_016866593.1:p.Arg954Pro
XM_017011105.2:c.2861G>C	XP_016866594.1:p.Arg954Pro
XM_017011106.2:c.2861G>C	XP_016866595.1:p.Arg954Pro
XM_017011107.2:c.2681G>C	XP_016866596.1:p.Arg894Pro
XR_002956289.1:n.2944G>C
NM_001363725.2:c.530G>C	NP_001350654.1:p.Arg177Pro
NM_001371656.1:c.3068G>C	NP_001358585.1:p.Arg1023Pro
NM_001374820.1:c.3068G>C	NP_001361749.1:p.Arg1023Pro
NM_001374828.1:c.3029G>C MANE Select	NP_001361757.1:p.Arg1010Pro
NM_017519.3:c.3029G>C	NP_059989.3:p.Arg1010Pro