Canonical Allele Identifier: CA366389145

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470007C>T (hg19) ; chr6:g.157148873C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148873C>T , CM000668.2:g.157148873C>T	GRCh38
NC_000006.11:g.157470007C>T , CM000668.1:g.157470007C>T	GRCh37
NC_000006.10:g.157511699C>T	NCBI36
NG_032093.1:g.375944C>T
NG_032093.2:g.375944C>T
NG_066624.1:g.377848C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3011C>T	ENSP00000055163.8:p.Pro1004Leu
ENST00000414678.8:c.2921C>T	ENSP00000412835.3:p.Pro974Leu
ENST00000637015.2:c.3011C>T	ENSP00000489729.2:p.Pro1004Leu
ENST00000319584.11:c.1025C>T	ENSP00000313006.7:p.Pro342Leu
ENST00000346085.10:c.3050C>T	ENSP00000344546.5:p.Pro1017Leu
ENST00000350026.10:c.2762C>T	ENSP00000055163.7:p.Pro921Leu
ENST00000414678.7:c.1169C>T	ENSP00000412835.2:p.Pro390Leu
ENST00000452544.2:n.912C>T
ENST00000635849.1:c.332C>T	ENSP00000490948.1:p.Pro111Leu
ENST00000636426.1:n.145C>T
ENST00000636930.2:c.3011C>T MANE Select	ENSP00000490491.2:p.Pro1004Leu
ENST00000637015.1:c.250C>T
ENST00000637568.1:c.54C>T
ENST00000637810.1:c.512C>T	ENSP00000489636.1:p.Pro171Leu
ENST00000637904.1:c.512C>T	ENSP00000490550.1:p.Pro171Leu
ENST00000647938.1:c.2801C>T	ENSP00000498155.1:p.Pro934Leu
ENST00000674190.1:n.1760C>T
ENST00000319584.10:c.1028C>T	ENSP00000313006.6:p.Pro343Leu
ENST00000346085.9:c.2801C>T	ENSP00000344546.4:p.Pro934Leu
ENST00000350026.9:c.2762C>T	ENSP00000055163.7:p.Pro921Leu
ENST00000414678.6:c.1169C>T	ENSP00000412835.2:p.Pro390Leu
ENST00000452544.1:n.858C>T
ENST00000478761.3:c.84C>T
NM_017519.2:c.2762C>T	NP_059989.2:p.Pro921Leu
NM_020732.3:c.2801C>T	NP_065783.3:p.Pro934Leu
XM_005267069.3:c.2762C>T	XP_005267126.2:p.Pro921Leu
XM_011535984.1:c.1712C>T	XP_011534286.1:p.Pro571Leu
XM_011535985.1:c.1532C>T	XP_011534287.1:p.Pro511Leu
XM_011535986.1:c.1292C>T	XP_011534288.1:p.Pro431Leu
XM_011535987.1:c.911C>T	XP_011534289.1:p.Pro304Leu
XM_011535988.1:c.-20+15666C>T	XP_011534290.1:n.-20+15666C>T
NM_001346813.1:c.2762C>T	NP_001333742.1:p.Pro921Leu
NM_001363725.1:c.512C>T	NP_001350654.1:p.Pro171Leu
XM_011535984.2:c.2843C>T	XP_011534286.2:p.Pro948Leu
XM_011535988.3:c.-20+15666C>T	XP_011534290.1:n.-20+15666C>T
XM_017011103.2:c.2843C>T	XP_016866592.1:p.Pro948Leu
XM_017011104.1:c.2843C>T	XP_016866593.1:p.Pro948Leu
XM_017011105.2:c.2843C>T	XP_016866594.1:p.Pro948Leu
XM_017011106.2:c.2843C>T	XP_016866595.1:p.Pro948Leu
XM_017011107.2:c.2663C>T	XP_016866596.1:p.Pro888Leu
XR_002956289.1:n.2926C>T
NM_001363725.2:c.512C>T	NP_001350654.1:p.Pro171Leu
NM_001371656.1:c.3050C>T	NP_001358585.1:p.Pro1017Leu
NM_001374820.1:c.3050C>T	NP_001361749.1:p.Pro1017Leu
NM_001374828.1:c.3011C>T MANE Select	NP_001361757.1:p.Pro1004Leu
NM_017519.3:c.3011C>T	NP_059989.3:p.Pro1004Leu