Canonical Allele Identifier: CA366389064

Gene: ARID1B

Linked Data

• dbSNP Id: rs1379941598
• gnomAD v4: 6-157148836-G-C
• MyVariant Identifiers: chr6:g.157469970G>C (hg19) ; chr6:g.157148836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148836G>C , CM000668.2:g.157148836G>C	GRCh38
NC_000006.11:g.157469970G>C , CM000668.1:g.157469970G>C	GRCh37
NC_000006.10:g.157511662G>C	NCBI36
NG_032093.1:g.375907G>C
NG_032093.2:g.375907G>C
NG_066624.1:g.377811G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2974G>C	ENSP00000055163.8:p.Gly992Arg
ENST00000414678.8:c.2884G>C	ENSP00000412835.3:p.Gly962Arg
ENST00000637015.2:c.2974G>C	ENSP00000489729.2:p.Gly992Arg
ENST00000319584.11:c.988G>C	ENSP00000313006.7:p.Gly330Arg
ENST00000346085.10:c.3013G>C	ENSP00000344546.5:p.Gly1005Arg
ENST00000350026.10:c.2725G>C	ENSP00000055163.7:p.Gly909Arg
ENST00000414678.7:c.1132G>C	ENSP00000412835.2:p.Gly378Arg
ENST00000452544.2:n.875G>C
ENST00000635849.1:c.295G>C	ENSP00000490948.1:p.Gly99Arg
ENST00000636426.1:n.108G>C
ENST00000636930.2:c.2974G>C MANE Select	ENSP00000490491.2:p.Gly992Arg
ENST00000637015.1:c.213G>C
ENST00000637568.1:c.17G>C
ENST00000637810.1:c.475G>C	ENSP00000489636.1:p.Gly159Arg
ENST00000637904.1:c.475G>C	ENSP00000490550.1:p.Gly159Arg
ENST00000647938.1:c.2764G>C	ENSP00000498155.1:p.Gly922Arg
ENST00000674190.1:n.1723G>C
ENST00000319584.10:c.991G>C	ENSP00000313006.6:p.Gly331Arg
ENST00000346085.9:c.2764G>C	ENSP00000344546.4:p.Gly922Arg
ENST00000350026.9:c.2725G>C	ENSP00000055163.7:p.Gly909Arg
ENST00000414678.6:c.1132G>C	ENSP00000412835.2:p.Gly378Arg
ENST00000452544.1:n.821G>C
ENST00000478761.3:c.47G>C
NM_017519.2:c.2725G>C	NP_059989.2:p.Gly909Arg
NM_020732.3:c.2764G>C	NP_065783.3:p.Gly922Arg
XM_005267069.3:c.2725G>C	XP_005267126.2:p.Gly909Arg
XM_011535984.1:c.1675G>C	XP_011534286.1:p.Gly559Arg
XM_011535985.1:c.1495G>C	XP_011534287.1:p.Gly499Arg
XM_011535986.1:c.1255G>C	XP_011534288.1:p.Gly419Arg
XM_011535987.1:c.874G>C	XP_011534289.1:p.Gly292Arg
XM_011535988.1:c.-20+15629G>C	XP_011534290.1:n.-20+15629G>C
NM_001346813.1:c.2725G>C	NP_001333742.1:p.Gly909Arg
NM_001363725.1:c.475G>C	NP_001350654.1:p.Gly159Arg
XM_011535984.2:c.2806G>C	XP_011534286.2:p.Gly936Arg
XM_011535988.3:c.-20+15629G>C	XP_011534290.1:n.-20+15629G>C
XM_017011103.2:c.2806G>C	XP_016866592.1:p.Gly936Arg
XM_017011104.1:c.2806G>C	XP_016866593.1:p.Gly936Arg
XM_017011105.2:c.2806G>C	XP_016866594.1:p.Gly936Arg
XM_017011106.2:c.2806G>C	XP_016866595.1:p.Gly936Arg
XM_017011107.2:c.2626G>C	XP_016866596.1:p.Gly876Arg
XR_002956289.1:n.2889G>C
NM_001363725.2:c.475G>C	NP_001350654.1:p.Gly159Arg
NM_001371656.1:c.3013G>C	NP_001358585.1:p.Gly1005Arg
NM_001374820.1:c.3013G>C	NP_001361749.1:p.Gly1005Arg
NM_001374828.1:c.2974G>C MANE Select	NP_001361757.1:p.Gly992Arg
NM_017519.3:c.2974G>C	NP_059989.3:p.Gly992Arg