Canonical Allele Identifier: CA515747718
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs1435192997
gnomAD v2: X-25022751-G-A
gnomAD v3: X-25004634-G-A
gnomAD v4: X-25004634-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004634G>A , CM000685.2:g.25004634G>A GRCh38
NC_000023.10:g.25022751G>A , CM000685.1:g.25022751G>A GRCh37
NC_000023.9:g.24932672G>A NCBI36
NG_008281.1:g.16315C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.*36C>T MANE Select ENSP00000368332.4:n.*36C>T
ENST00000379044.4:c.*36C>T ENSP00000368332.4:n.*36C>T
NM_139058.2:c.*36C>T NP_620689.1:n.*36C>T
NM_139058.3:c.*36C>T MANE Select NP_620689.1:n.*36C>T