Canonical Allele Identifier: CA645160467
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs782429090
gnomAD v2: X-153002564-C-G
gnomAD v4: X-153737110-C-G
MyVariant Identifiers: chrX:g.153002564C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153737110C>G , CM000685.2:g.153737110C>G GRCh38
NC_000023.10:g.153002564C>G , CM000685.1:g.153002564C>G GRCh37
NC_000023.9:g.152655758C>G NCBI36
NG_009022.2:g.17243C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1394-47C>G MANE Select ENSP00000218104.3:n.1394-47C>G
ENST00000218104.5:c.1394-47C>G ENSP00000218104.3:n.1394-47C>G
ENST00000443684.2:n.397-47C>G
NM_000033.3:c.1394-47C>G NP_000024.2:n.1394-47C>G
XR_938507.1:n.1866-47C>G
XR_938507.2:n.1866-47C>G
NM_000033.4:c.1394-47C>G MANE Select NP_000024.2:n.1394-47C>G
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