Canonical Allele Identifier: CA366242584

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522466A>T (hg19) ; chr6:g.157201332A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201332A>T , CM000668.2:g.157201332A>T	GRCh38
NC_000006.11:g.157522466A>T , CM000668.1:g.157522466A>T	GRCh37
NC_000006.10:g.157564158A>T	NCBI36
NG_032093.1:g.428403A>T
NG_032093.2:g.428403A>T
NG_066624.1:g.430307A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4948A>T	ENSP00000055163.8:p.Met1650Leu
ENST00000414678.8:c.5017A>T	ENSP00000412835.3:p.Met1673Leu
ENST00000637015.2:c.5236A>T	ENSP00000489729.2:p.Met1746Leu
ENST00000346085.10:c.4987A>T	ENSP00000344546.5:p.Met1663Leu
ENST00000350026.10:c.4699A>T	ENSP00000055163.7:p.Met1567Leu
ENST00000414678.7:c.3265A>T	ENSP00000412835.2:p.Met1089Leu
ENST00000635849.1:c.2428A>T	ENSP00000490948.1:p.Met810Leu
ENST00000635957.1:c.2059A>T	ENSP00000490385.1:p.Met687Leu
ENST00000636227.1:n.3570A>T
ENST00000636254.1:n.1027A>T
ENST00000636930.2:c.5107A>T MANE Select	ENSP00000490491.2:p.Met1703Leu
ENST00000636940.1:n.3104A>T
ENST00000637015.1:c.2475A>T
ENST00000637568.1:c.2389A>T
ENST00000637741.1:n.1773A>T
ENST00000637810.1:c.2449A>T	ENSP00000489636.1:p.Met817Leu
ENST00000637904.1:c.2608A>T	ENSP00000490550.1:p.Met870Leu
ENST00000647938.1:c.4738A>T	ENSP00000498155.1:p.Met1580Leu
ENST00000346085.9:c.4738A>T	ENSP00000344546.4:p.Met1580Leu
ENST00000350026.9:c.4699A>T	ENSP00000055163.7:p.Met1567Leu
ENST00000414678.6:c.3265A>T	ENSP00000412835.2:p.Met1089Leu
NM_017519.2:c.4699A>T	NP_059989.2:p.Met1567Leu
NM_020732.3:c.4738A>T	NP_065783.3:p.Met1580Leu
XM_005267069.3:c.4858A>T	XP_005267126.2:p.Met1620Leu
XM_011535984.1:c.3937A>T	XP_011534286.1:p.Met1313Leu
XM_011535985.1:c.3757A>T	XP_011534287.1:p.Met1253Leu
XM_011535986.1:c.3517A>T	XP_011534288.1:p.Met1173Leu
XM_011535987.1:c.3136A>T	XP_011534289.1:p.Met1046Leu
XM_011535988.1:c.1999A>T	XP_011534290.1:p.Met667Leu
NM_001346813.1:c.4858A>T	NP_001333742.1:p.Met1620Leu
NM_001363725.1:c.2608A>T	NP_001350654.1:p.Met870Leu
XM_011535984.2:c.5068A>T	XP_011534286.2:p.Met1690Leu
XM_011535988.3:c.1999A>T	XP_011534290.1:p.Met667Leu
XM_017011103.2:c.4969A>T	XP_016866592.1:p.Met1657Leu
XM_017011104.1:c.4939A>T	XP_016866593.1:p.Met1647Leu
XM_017011105.2:c.4909A>T	XP_016866594.1:p.Met1637Leu
XM_017011106.2:c.4780A>T	XP_016866595.1:p.Met1594Leu
XM_017011107.2:c.4759A>T	XP_016866596.1:p.Met1587Leu
XR_002956289.1:n.5054A>T
NM_001363725.2:c.2608A>T	NP_001350654.1:p.Met870Leu
NM_001371656.1:c.4987A>T	NP_001358585.1:p.Met1663Leu
NM_001374820.1:c.4987A>T	NP_001361749.1:p.Met1663Leu
NM_001374828.1:c.5107A>T MANE Select	NP_001361757.1:p.Met1703Leu
NM_017519.3:c.4948A>T	NP_059989.3:p.Met1650Leu