Canonical Allele Identifier: CA337240303
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs782243754
gnomAD v4: X-153737118-C-G
MyVariant Identifiers: chrX:g.153002572C>G (hg19) chrX:g.153737118C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153737118C>G , CM000685.2:g.153737118C>G GRCh38
NC_000023.10:g.153002572C>G , CM000685.1:g.153002572C>G GRCh37
NC_000023.9:g.152655766C>G NCBI36
NG_009022.2:g.17251C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1394-39C>G MANE Select ENSP00000218104.3:n.1394-39C>G
ENST00000218104.5:c.1394-39C>G ENSP00000218104.3:n.1394-39C>G
ENST00000443684.2:n.397-39C>G
NM_000033.3:c.1394-39C>G NP_000024.2:n.1394-39C>G
XR_938507.1:n.1866-39C>G
XR_938507.2:n.1866-39C>G
NM_000033.4:c.1394-39C>G MANE Select NP_000024.2:n.1394-39C>G
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