Canonical Allele Identifier: CA873270974
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1283735339
gnomAD v3: X-153742806-G-C
gnomAD v4: X-153742806-G-C
MyVariant Identifiers: chrX:g.153742806G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742806G>C , CM000685.2:g.153742806G>C GRCh38
NC_000023.10:g.153008260G>C , CM000685.1:g.153008260G>C GRCh37
NC_000023.9:g.152661454G>C NCBI36
NG_009022.2:g.22939G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1781-181G>C MANE Select ENSP00000218104.3:n.1781-181G>C
ENST00000218104.5:c.1781-181G>C ENSP00000218104.3:n.1781-181G>C
NM_000033.3:c.1781-181G>C NP_000024.2:n.1781-181G>C
XR_938507.1:n.2253-181G>C
XR_938507.2:n.2253-181G>C
NM_000033.4:c.1781-181G>C MANE Select NP_000024.2:n.1781-181G>C
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