Canonical Allele Identifier: CA645288162
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1557055199
gnomAD v2: X-153008357-A-G
gnomAD v3: X-153742903-A-G
gnomAD v4: X-153742903-A-G
MyVariant Identifiers: chrX:g.153008357A>G (hg19) chrX:g.153742903A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742903A>G , CM000685.2:g.153742903A>G GRCh38
NC_000023.10:g.153008357A>G , CM000685.1:g.153008357A>G GRCh37
NC_000023.9:g.152661551A>G NCBI36
NG_009022.2:g.23036A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1781-84A>G MANE Select ENSP00000218104.3:n.1781-84A>G
ENST00000218104.5:c.1781-84A>G ENSP00000218104.3:n.1781-84A>G
NM_000033.3:c.1781-84A>G NP_000024.2:n.1781-84A>G
XR_938507.1:n.2253-84A>G
XR_938507.2:n.2253-84A>G
NM_000033.4:c.1781-84A>G MANE Select NP_000024.2:n.1781-84A>G
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