Canonical Allele Identifier: CA384609138

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45730061T>G , CM000674.2:g.45730061T>G	GRCh38
NC_000012.11:g.46123844T>G , CM000674.1:g.46123844T>G	GRCh37
NC_000012.10:g.44410111T>G	NCBI36
NG_052800.1:g.5397T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.110T>G	ENSP00000415650.3:p.Ile37Ser
ENST00000700074.1:n.241T>G
ENST00000334344.11:c.110T>G MANE Select	ENSP00000335044.6:p.Ile37Ser
ENST00000422737.6:c.31T>G
ENST00000334344.10:c.110T>G	ENSP00000335044.6:p.Ile37Ser
ENST00000422737.5:c.-338T>G	ENSP00000415650.1:n.-338T>G
ENST00000426776.5:n.61T>G
ENST00000427628.5:n.74T>G
NM_152641.2:c.110T>G	NP_689854.2:p.Ile37Ser
XM_006719272.2:c.110T>G	XP_006719335.1:p.Ile37Ser
XR_944505.1:n.258T>G
NM_001347839.1:c.110T>G	NP_001334768.1:p.Ile37Ser
NM_152641.3:c.110T>G	NP_689854.2:p.Ile37Ser
XM_006719272.4:c.110T>G	XP_006719335.1:p.Ile37Ser
XR_944505.3:n.241T>G
NM_152641.4:c.110T>G MANE Select	NP_689854.2:p.Ile37Ser
NM_001347839.2:c.110T>G	NP_001334768.1:p.Ile37Ser