Canonical Allele Identifier: CA645288157
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1248514684
gnomAD v2: X-153008315-A-G
gnomAD v3: X-153742861-A-G
gnomAD v4: X-153742861-A-G
MyVariant Identifiers: chrX:g.153008315A>G (hg19) chrX:g.153742861A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742861A>G , CM000685.2:g.153742861A>G GRCh38
NC_000023.10:g.153008315A>G , CM000685.1:g.153008315A>G GRCh37
NC_000023.9:g.152661509A>G NCBI36
NG_009022.2:g.22994A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1781-126A>G MANE Select ENSP00000218104.3:n.1781-126A>G
ENST00000218104.5:c.1781-126A>G ENSP00000218104.3:n.1781-126A>G
NM_000033.3:c.1781-126A>G NP_000024.2:n.1781-126A>G
XR_938507.1:n.2253-126A>G
XR_938507.2:n.2253-126A>G
NM_000033.4:c.1781-126A>G MANE Select NP_000024.2:n.1781-126A>G
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