Canonical Allele Identifier: CA10550297
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs782803612
ExAC: X:153006127 C / G
gnomAD v4: X-153740673-C-G
MyVariant Identifiers: chrX:g.153006127C>G (hg19) chrX:g.153740673C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740673C>G , CM000685.2:g.153740673C>G GRCh38
NC_000023.10:g.153006127C>G , CM000685.1:g.153006127C>G GRCh37
NC_000023.9:g.152659321C>G NCBI36
NG_009022.2:g.20806C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1734C>G MANE Select ENSP00000218104.3:p.Ala578=
ENST00000218104.5:c.1734C>G ENSP00000218104.3:p.Ala578=
NM_000033.3:c.1734C>G NP_000024.2:p.Ala578=
XR_938507.1:n.2206C>G
XR_938507.2:n.2206C>G
NM_000033.4:c.1734C>G MANE Select NP_000024.2:p.Ala578=
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Search 100 bp 3'