Canonical Allele Identifier: CA344935349

Gene: ARID4B

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235175183C>A , CM000663.2:g.235175183C>A	GRCh38
NC_000001.10:g.235338498C>A , CM000663.1:g.235338498C>A	GRCh37
NC_000001.9:g.233405121C>A	NCBI36
NG_029484.1:g.158035G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264183.9:c.3664+1G>T MANE Select	ENSP00000264183.3:n.3664+1G>T
ENST00000264183.7:c.3664+1G>T	ENSP00000264183.3:n.3664+1G>T
ENST00000349213.7:c.3406+1G>T	ENSP00000264184.4:n.3406+1G>T
ENST00000366603.6:c.3664+1G>T	ENSP00000355562.2:n.3664+1G>T
ENST00000421364.5:c.*358+1G>T	ENSP00000394663.1:n.*358+1G>T
ENST00000474401.1:n.460+1G>T
ENST00000474953.5:c.1604+1G>T
NM_001206794.1:c.3664+1G>T	NP_001193723.1:n.3664+1G>T
NM_016374.5:c.3664+1G>T	NP_057458.4:n.3664+1G>T
NM_031371.3:c.3406+1G>T	NP_112739.2:n.3406+1G>T
XM_006711781.1:c.3556+1G>T	XP_006711844.1:n.3556+1G>T
XM_011544212.1:c.3664+1G>T	XP_011542514.1:n.3664+1G>T
XM_011544213.1:c.2785+1G>T	XP_011542515.1:n.2785+1G>T
XR_949145.1:n.4303+1G>T
NR_135074.1:n.4320+1G>T
XM_006711781.3:c.3556+1G>T	XP_006711844.1:n.3556+1G>T
XM_011544212.3:c.3664+1G>T	XP_011542514.1:n.3664+1G>T
XM_017001472.1:c.2785+1G>T	XP_016856961.1:n.2785+1G>T
XM_024447626.1:c.3406+1G>T	XP_024303394.1:n.3406+1G>T
XR_001737226.2:n.4241+1G>T
XR_001737227.2:n.4175+1G>T
XR_002956802.1:n.3983+1G>T
NM_016374.6:c.3664+1G>T MANE Select	NP_057458.4:n.3664+1G>T
NM_031371.4:c.3406+1G>T	NP_112739.2:n.3406+1G>T
NR_135074.2:n.4280+1G>T
NM_001206794.2:c.3664+1G>T	NP_001193723.1:n.3664+1G>T