Canonical Allele Identifier: CA2680921224

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157173932-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157173932G>T , CM000668.2:g.157173932G>T	GRCh38
NC_000006.11:g.157495066G>T , CM000668.1:g.157495066G>T	GRCh37
NC_000006.10:g.157536758G>T	NCBI36
NG_032093.1:g.401003G>T
NG_032093.2:g.401003G>T
NG_066624.1:g.402907G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3236-76G>T	ENSP00000055163.8:n.3236-76G>T
ENST00000414678.8:c.3146-76G>T	ENSP00000412835.3:n.3146-76G>T
ENST00000637015.2:c.3365-76G>T	ENSP00000489729.2:n.3365-76G>T
ENST00000319584.11:c.1250-76G>T	ENSP00000313006.7:n.1250-76G>T
ENST00000346085.10:c.3275-76G>T	ENSP00000344546.5:n.3275-76G>T
ENST00000350026.10:c.2987-76G>T	ENSP00000055163.7:n.2987-76G>T
ENST00000414678.7:c.1394-76G>T	ENSP00000412835.2:n.1394-76G>T
ENST00000635849.1:c.557-76G>T	ENSP00000490948.1:n.557-76G>T
ENST00000635957.1:c.191-76G>T	ENSP00000490385.1:n.191-76G>T
ENST00000636930.2:c.3236-76G>T MANE Select	ENSP00000490491.2:n.3236-76G>T
ENST00000636940.1:n.1157G>T
ENST00000637015.1:c.604-76G>T
ENST00000637170.1:n.432G>T
ENST00000637568.1:c.518-76G>T
ENST00000637741.1:n.61-76G>T
ENST00000637810.1:c.737-76G>T	ENSP00000489636.1:n.737-76G>T
ENST00000637904.1:c.737-76G>T	ENSP00000490550.1:n.737-76G>T
ENST00000647938.1:c.3026-76G>T	ENSP00000498155.1:n.3026-76G>T
ENST00000319584.10:c.1253-76G>T	ENSP00000313006.6:n.1253-76G>T
ENST00000346085.9:c.3026-76G>T	ENSP00000344546.4:n.3026-76G>T
ENST00000350026.9:c.2987-76G>T	ENSP00000055163.7:n.2987-76G>T
ENST00000400790.3:c.188-76G>T	ENSP00000383596.3:n.188-76G>T
ENST00000414678.6:c.1394-76G>T	ENSP00000412835.2:n.1394-76G>T
ENST00000478761.3:c.438-76G>T
NM_017519.2:c.2987-76G>T	NP_059989.2:n.2987-76G>T
NM_020732.3:c.3026-76G>T	NP_065783.3:n.3026-76G>T
XM_005267069.3:c.2987-76G>T	XP_005267126.2:n.2987-76G>T
XM_011535984.1:c.2066-76G>T	XP_011534286.1:n.2066-76G>T
XM_011535985.1:c.1886-76G>T	XP_011534287.1:n.1886-76G>T
XM_011535986.1:c.1646-76G>T	XP_011534288.1:n.1646-76G>T
XM_011535987.1:c.1265-76G>T	XP_011534289.1:n.1265-76G>T
XM_011535988.1:c.128-76G>T	XP_011534290.1:n.128-76G>T
NM_001346813.1:c.2987-76G>T	NP_001333742.1:n.2987-76G>T
NM_001363725.1:c.737-76G>T	NP_001350654.1:n.737-76G>T
XM_011535984.2:c.3197-76G>T	XP_011534286.2:n.3197-76G>T
XM_011535988.3:c.128-76G>T	XP_011534290.1:n.128-76G>T
XM_017011103.2:c.3098-76G>T	XP_016866592.1:n.3098-76G>T
XM_017011104.1:c.3068-76G>T	XP_016866593.1:n.3068-76G>T
XM_017011105.2:c.3197-76G>T	XP_016866594.1:n.3197-76G>T
XM_017011106.2:c.3068-76G>T	XP_016866595.1:n.3068-76G>T
XM_017011107.2:c.2888-76G>T	XP_016866596.1:n.2888-76G>T
XR_002956289.1:n.3280-76G>T
NM_001363725.2:c.737-76G>T	NP_001350654.1:n.737-76G>T
NM_001371656.1:c.3275-76G>T	NP_001358585.1:n.3275-76G>T
NM_001374820.1:c.3275-76G>T	NP_001361749.1:n.3275-76G>T
NM_001374828.1:c.3236-76G>T MANE Select	NP_001361757.1:n.3236-76G>T
NM_017519.3:c.3236-76G>T	NP_059989.3:n.3236-76G>T