Canonical Allele Identifier: CA645288089
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1557054199
gnomAD v2: X-153001770-G-A
MyVariant Identifiers: chrX:g.153001770G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736316G>A , CM000685.2:g.153736316G>A GRCh38
NC_000023.10:g.153001770G>A , CM000685.1:g.153001770G>A GRCh37
NC_000023.9:g.152654964G>A NCBI36
NG_009022.2:g.16449G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1225-29G>A MANE Select ENSP00000218104.3:n.1225-29G>A
ENST00000218104.5:c.1225-29G>A ENSP00000218104.3:n.1225-29G>A
ENST00000443684.2:n.228-29G>A
NM_000033.3:c.1225-29G>A NP_000024.2:n.1225-29G>A
XR_938507.1:n.1641-29G>A
XR_938507.2:n.1641-29G>A
NM_000033.4:c.1225-29G>A MANE Select NP_000024.2:n.1225-29G>A
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