Canonical Allele Identifier: CA366389263

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470063G>T (hg19) ; chr6:g.157148929G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148929G>T , CM000668.2:g.157148929G>T	GRCh38
NC_000006.11:g.157470063G>T , CM000668.1:g.157470063G>T	GRCh37
NC_000006.10:g.157511755G>T	NCBI36
NG_032093.1:g.376000G>T
NG_032093.2:g.376000G>T
NG_066624.1:g.377904G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3067G>T	ENSP00000055163.8:p.Ala1023Ser
ENST00000414678.8:c.2977G>T	ENSP00000412835.3:p.Ala993Ser
ENST00000637015.2:c.3067G>T	ENSP00000489729.2:p.Ala1023Ser
ENST00000319584.11:c.1081G>T	ENSP00000313006.7:p.Ala361Ser
ENST00000346085.10:c.3106G>T	ENSP00000344546.5:p.Ala1036Ser
ENST00000350026.10:c.2818G>T	ENSP00000055163.7:p.Ala940Ser
ENST00000414678.7:c.1225G>T	ENSP00000412835.2:p.Ala409Ser
ENST00000452544.2:n.968G>T
ENST00000635849.1:c.388G>T	ENSP00000490948.1:p.Ala130Ser
ENST00000635957.1:c.22G>T	ENSP00000490385.1:p.Ala8Ser
ENST00000636426.1:n.201G>T
ENST00000636930.2:c.3067G>T MANE Select	ENSP00000490491.2:p.Ala1023Ser
ENST00000637015.1:c.306G>T
ENST00000637568.1:c.110G>T
ENST00000637810.1:c.568G>T	ENSP00000489636.1:p.Ala190Ser
ENST00000637904.1:c.568G>T	ENSP00000490550.1:p.Ala190Ser
ENST00000647938.1:c.2857G>T	ENSP00000498155.1:p.Ala953Ser
ENST00000674190.1:n.1816G>T
ENST00000319584.10:c.1084G>T	ENSP00000313006.6:p.Ala362Ser
ENST00000346085.9:c.2857G>T	ENSP00000344546.4:p.Ala953Ser
ENST00000350026.9:c.2818G>T	ENSP00000055163.7:p.Ala940Ser
ENST00000400790.3:c.19G>T	ENSP00000383596.3:p.Ala7Ser
ENST00000414678.6:c.1225G>T	ENSP00000412835.2:p.Ala409Ser
ENST00000452544.1:n.914G>T
ENST00000478761.3:c.140G>T
NM_017519.2:c.2818G>T	NP_059989.2:p.Ala940Ser
NM_020732.3:c.2857G>T	NP_065783.3:p.Ala953Ser
XM_005267069.3:c.2818G>T	XP_005267126.2:p.Ala940Ser
XM_011535984.1:c.1768G>T	XP_011534286.1:p.Ala590Ser
XM_011535985.1:c.1588G>T	XP_011534287.1:p.Ala530Ser
XM_011535986.1:c.1348G>T	XP_011534288.1:p.Ala450Ser
XM_011535987.1:c.967G>T	XP_011534289.1:p.Ala323Ser
XM_011535988.1:c.-20+15722G>T	XP_011534290.1:n.-20+15722G>T
NM_001346813.1:c.2818G>T	NP_001333742.1:p.Ala940Ser
NM_001363725.1:c.568G>T	NP_001350654.1:p.Ala190Ser
XM_011535984.2:c.2899G>T	XP_011534286.2:p.Ala967Ser
XM_011535988.3:c.-20+15722G>T	XP_011534290.1:n.-20+15722G>T
XM_017011103.2:c.2899G>T	XP_016866592.1:p.Ala967Ser
XM_017011104.1:c.2899G>T	XP_016866593.1:p.Ala967Ser
XM_017011105.2:c.2899G>T	XP_016866594.1:p.Ala967Ser
XM_017011106.2:c.2899G>T	XP_016866595.1:p.Ala967Ser
XM_017011107.2:c.2719G>T	XP_016866596.1:p.Ala907Ser
XR_002956289.1:n.2982G>T
NM_001363725.2:c.568G>T	NP_001350654.1:p.Ala190Ser
NM_001371656.1:c.3106G>T	NP_001358585.1:p.Ala1036Ser
NM_001374820.1:c.3106G>T	NP_001361749.1:p.Ala1036Ser
NM_001374828.1:c.3067G>T MANE Select	NP_001361757.1:p.Ala1023Ser
NM_017519.3:c.3067G>T	NP_059989.3:p.Ala1023Ser