Canonical Allele Identifier: CA366389247

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470055T>G (hg19) ; chr6:g.157148921T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148921T>G , CM000668.2:g.157148921T>G	GRCh38
NC_000006.11:g.157470055T>G , CM000668.1:g.157470055T>G	GRCh37
NC_000006.10:g.157511747T>G	NCBI36
NG_032093.1:g.375992T>G
NG_032093.2:g.375992T>G
NG_066624.1:g.377896T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3059T>G	ENSP00000055163.8:p.Met1020Arg
ENST00000414678.8:c.2969T>G	ENSP00000412835.3:p.Met990Arg
ENST00000637015.2:c.3059T>G	ENSP00000489729.2:p.Met1020Arg
ENST00000319584.11:c.1073T>G	ENSP00000313006.7:p.Met358Arg
ENST00000346085.10:c.3098T>G	ENSP00000344546.5:p.Met1033Arg
ENST00000350026.10:c.2810T>G	ENSP00000055163.7:p.Met937Arg
ENST00000414678.7:c.1217T>G	ENSP00000412835.2:p.Met406Arg
ENST00000452544.2:n.960T>G
ENST00000635849.1:c.380T>G	ENSP00000490948.1:p.Met127Arg
ENST00000635957.1:c.14T>G	ENSP00000490385.1:p.Met5Arg
ENST00000636426.1:n.193T>G
ENST00000636930.2:c.3059T>G MANE Select	ENSP00000490491.2:p.Met1020Arg
ENST00000637015.1:c.298T>G
ENST00000637568.1:c.102T>G
ENST00000637810.1:c.560T>G	ENSP00000489636.1:p.Met187Arg
ENST00000637904.1:c.560T>G	ENSP00000490550.1:p.Met187Arg
ENST00000647938.1:c.2849T>G	ENSP00000498155.1:p.Met950Arg
ENST00000674190.1:n.1808T>G
ENST00000319584.10:c.1076T>G	ENSP00000313006.6:p.Met359Arg
ENST00000346085.9:c.2849T>G	ENSP00000344546.4:p.Met950Arg
ENST00000350026.9:c.2810T>G	ENSP00000055163.7:p.Met937Arg
ENST00000400790.3:c.11T>G	ENSP00000383596.3:p.Met4Arg
ENST00000414678.6:c.1217T>G	ENSP00000412835.2:p.Met406Arg
ENST00000452544.1:n.906T>G
ENST00000478761.3:c.132T>G
NM_017519.2:c.2810T>G	NP_059989.2:p.Met937Arg
NM_020732.3:c.2849T>G	NP_065783.3:p.Met950Arg
XM_005267069.3:c.2810T>G	XP_005267126.2:p.Met937Arg
XM_011535984.1:c.1760T>G	XP_011534286.1:p.Met587Arg
XM_011535985.1:c.1580T>G	XP_011534287.1:p.Met527Arg
XM_011535986.1:c.1340T>G	XP_011534288.1:p.Met447Arg
XM_011535987.1:c.959T>G	XP_011534289.1:p.Met320Arg
XM_011535988.1:c.-20+15714T>G	XP_011534290.1:n.-20+15714T>G
NM_001346813.1:c.2810T>G	NP_001333742.1:p.Met937Arg
NM_001363725.1:c.560T>G	NP_001350654.1:p.Met187Arg
XM_011535984.2:c.2891T>G	XP_011534286.2:p.Met964Arg
XM_011535988.3:c.-20+15714T>G	XP_011534290.1:n.-20+15714T>G
XM_017011103.2:c.2891T>G	XP_016866592.1:p.Met964Arg
XM_017011104.1:c.2891T>G	XP_016866593.1:p.Met964Arg
XM_017011105.2:c.2891T>G	XP_016866594.1:p.Met964Arg
XM_017011106.2:c.2891T>G	XP_016866595.1:p.Met964Arg
XM_017011107.2:c.2711T>G	XP_016866596.1:p.Met904Arg
XR_002956289.1:n.2974T>G
NM_001363725.2:c.560T>G	NP_001350654.1:p.Met187Arg
NM_001371656.1:c.3098T>G	NP_001358585.1:p.Met1033Arg
NM_001374820.1:c.3098T>G	NP_001361749.1:p.Met1033Arg
NM_001374828.1:c.3059T>G MANE Select	NP_001361757.1:p.Met1020Arg
NM_017519.3:c.3059T>G	NP_059989.3:p.Met1020Arg