Canonical Allele Identifier: CA10373872
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs780415621
gnomAD v2: X-25031279-G-C
gnomAD v4: X-25013162-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013162G>C , CM000685.2:g.25013162G>C GRCh38
NC_000023.10:g.25031279G>C , CM000685.1:g.25031279G>C GRCh37
NC_000023.9:g.24941200G>C NCBI36
NG_008281.1:g.7787C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.833C>G MANE Select ENSP00000368332.4:p.Ala278Gly
ENST00000379044.4:c.833C>G ENSP00000368332.4:p.Ala278Gly
NM_139058.2:c.833C>G NP_620689.1:p.Ala278Gly
NM_139058.3:c.833C>G MANE Select NP_620689.1:p.Ala278Gly