Canonical Allele Identifier: CA384492143
Gene: ARID2 HGNC NCBI

Linked Data

dbSNP Id: rs1943579690

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852759A>C , CM000674.2:g.45852759A>C GRCh38
NC_000012.11:g.46246542A>C , CM000674.1:g.46246542A>C GRCh37
NC_000012.10:g.44532809A>C NCBI36
NG_052800.1:g.128095A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4636A>C ENSP00000415650.3:p.Asn1546His
ENST00000457135.2:c.845A>C
ENST00000334344.11:c.4636A>C MANE Select ENSP00000335044.6:p.Asn1546His
ENST00000422737.6:c.4557A>C
ENST00000334344.10:c.4636A>C ENSP00000335044.6:p.Asn1546His
ENST00000422737.5:c.4189A>C ENSP00000415650.1:p.Asn1397His
ENST00000444670.5:c.3466A>C ENSP00000397307.1:p.Asn1156His
ENST00000457135.1:c.460A>C ENSP00000388357.1:p.Asn154His
ENST00000479608.5:n.3927A>C
NM_152641.2:c.4636A>C NP_689854.2:p.Asn1546His
XM_006719272.2:c.4636A>C XP_006719335.1:p.Asn1546His
XM_011538025.1:c.3004A>C XP_011536327.1:p.Asn1002His
XR_944505.1:n.4784A>C
NM_001347839.1:c.4636A>C NP_001334768.1:p.Asn1546His
NM_152641.3:c.4636A>C NP_689854.2:p.Asn1546His
XM_006719272.4:c.4636A>C XP_006719335.1:p.Asn1546His
XR_944505.3:n.4767A>C
NM_152641.4:c.4636A>C MANE Select NP_689854.2:p.Asn1546His
NM_001347839.2:c.4636A>C NP_001334768.1:p.Asn1546His