Canonical Allele Identifier: CA873267603
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1263837318
gnomAD v3: X-153737069-T-G
gnomAD v4: X-153737069-T-G
MyVariant Identifiers: chrX:g.153737069T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153737069T>G , CM000685.2:g.153737069T>G GRCh38
NC_000023.10:g.153002523T>G , CM000685.1:g.153002523T>G GRCh37
NC_000023.9:g.152655717T>G NCBI36
NG_009022.2:g.17202T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1394-88T>G MANE Select ENSP00000218104.3:n.1394-88T>G
ENST00000218104.5:c.1394-88T>G ENSP00000218104.3:n.1394-88T>G
ENST00000443684.2:n.397-88T>G
NM_000033.3:c.1394-88T>G NP_000024.2:n.1394-88T>G
XR_938507.1:n.1866-88T>G
XR_938507.2:n.1866-88T>G
NM_000033.4:c.1394-88T>G MANE Select NP_000024.2:n.1394-88T>G
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