Canonical Allele Identifier: CA2420208014
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs778464180

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010212T>C , CM000685.2:g.25010212T>C GRCh38
NC_000023.10:g.25028329T>C , CM000685.1:g.25028329T>C GRCh37
NC_000023.9:g.24938250T>C NCBI36
NG_008281.1:g.10737A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+48A>G MANE Select ENSP00000368332.4:n.1119+48A>G
ENST00000379044.4:c.1119+48A>G ENSP00000368332.4:n.1119+48A>G
NM_139058.2:c.1119+48A>G NP_620689.1:n.1119+48A>G
NM_139058.3:c.1119+48A>G MANE Select NP_620689.1:n.1119+48A>G