Canonical Allele Identifier: CA10373860
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs769831204
gnomAD v2: X-25031089-C-T
gnomAD v4: X-25012972-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012972C>T , CM000685.2:g.25012972C>T GRCh38
NC_000023.10:g.25031089C>T , CM000685.1:g.25031089C>T GRCh37
NC_000023.9:g.24941010C>T NCBI36
NG_008281.1:g.7977G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1023G>A MANE Select ENSP00000368332.4:p.Glu341=
ENST00000379044.4:c.1023G>A ENSP00000368332.4:p.Glu341=
NM_139058.2:c.1023G>A NP_620689.1:p.Glu341=
NM_139058.3:c.1023G>A MANE Select NP_620689.1:p.Glu341=