Canonical Allele Identifier: CA366227375

Gene: ARID1B

Linked Data

• dbSNP Id: rs781714598
• MyVariant Identifiers: chr6:g.157502162T>G (hg19) ; chr6:g.157181028T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181028T>G , CM000668.2:g.157181028T>G	GRCh38
NC_000006.11:g.157502162T>G , CM000668.1:g.157502162T>G	GRCh37
NC_000006.10:g.157543854T>G	NCBI36
NG_032093.1:g.408099T>G
NG_032093.2:g.408099T>G
NG_066624.1:g.410003T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3405T>G	ENSP00000055163.8:p.Asn1135Lys
ENST00000414678.8:c.3474T>G	ENSP00000412835.3:p.Asn1158Lys
ENST00000637015.2:c.3693T>G	ENSP00000489729.2:p.Asn1231Lys
ENST00000319584.11:c.1578T>G	ENSP00000313006.7:p.Asn526Lys
ENST00000346085.10:c.3444T>G	ENSP00000344546.5:p.Asn1148Lys
ENST00000350026.10:c.3156T>G	ENSP00000055163.7:p.Asn1052Lys
ENST00000414678.7:c.1722T>G	ENSP00000412835.2:p.Asn574Lys
ENST00000635849.1:c.885T>G	ENSP00000490948.1:p.Asn295Lys
ENST00000635957.1:c.519T>G	ENSP00000490385.1:p.Asn173Lys
ENST00000636930.2:c.3564T>G MANE Select	ENSP00000490491.2:p.Asn1188Lys
ENST00000636940.1:n.1561T>G
ENST00000637015.1:c.932T>G
ENST00000637568.1:c.846T>G
ENST00000637741.1:n.230T>G
ENST00000637810.1:c.906T>G	ENSP00000489636.1:p.Asn302Lys
ENST00000637904.1:c.1065T>G	ENSP00000490550.1:p.Asn355Lys
ENST00000647938.1:c.3195T>G	ENSP00000498155.1:p.Asn1065Lys
ENST00000319584.10:c.1581T>G	ENSP00000313006.6:p.Asn527Lys
ENST00000346085.9:c.3195T>G	ENSP00000344546.4:p.Asn1065Lys
ENST00000350026.9:c.3156T>G	ENSP00000055163.7:p.Asn1052Lys
ENST00000400790.3:c.357T>G	ENSP00000383596.3:p.Asn119Lys
ENST00000414678.6:c.1722T>G	ENSP00000412835.2:p.Asn574Lys
ENST00000478761.3:c.766T>G
NM_017519.2:c.3156T>G	NP_059989.2:p.Asn1052Lys
NM_020732.3:c.3195T>G	NP_065783.3:p.Asn1065Lys
XM_005267069.3:c.3315T>G	XP_005267126.2:p.Asn1105Lys
XM_011535984.1:c.2394T>G	XP_011534286.1:p.Asn798Lys
XM_011535985.1:c.2214T>G	XP_011534287.1:p.Asn738Lys
XM_011535986.1:c.1974T>G	XP_011534288.1:p.Asn658Lys
XM_011535987.1:c.1593T>G	XP_011534289.1:p.Asn531Lys
XM_011535988.1:c.456T>G	XP_011534290.1:p.Asn152Lys
NM_001346813.1:c.3315T>G	NP_001333742.1:p.Asn1105Lys
NM_001363725.1:c.1065T>G	NP_001350654.1:p.Asn355Lys
XM_011535984.2:c.3525T>G	XP_011534286.2:p.Asn1175Lys
XM_011535988.3:c.456T>G	XP_011534290.1:p.Asn152Lys
XM_017011103.2:c.3426T>G	XP_016866592.1:p.Asn1142Lys
XM_017011104.1:c.3396T>G	XP_016866593.1:p.Asn1132Lys
XM_017011105.2:c.3366T>G	XP_016866594.1:p.Asn1122Lys
XM_017011106.2:c.3237T>G	XP_016866595.1:p.Asn1079Lys
XM_017011107.2:c.3216T>G	XP_016866596.1:p.Asn1072Lys
XR_002956289.1:n.3608T>G
NM_001363725.2:c.1065T>G	NP_001350654.1:p.Asn355Lys
NM_001371656.1:c.3444T>G	NP_001358585.1:p.Asn1148Lys
NM_001374820.1:c.3444T>G	NP_001361749.1:p.Asn1148Lys
NM_001374828.1:c.3564T>G MANE Select	NP_001361757.1:p.Asn1188Lys
NM_017519.3:c.3405T>G	NP_059989.3:p.Asn1135Lys