Canonical Allele Identifier: CA337242039
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs782252073
gnomAD v2: X-153006349-G-A
gnomAD v3: X-153740895-G-A
gnomAD v4: X-153740895-G-A
MyVariant Identifiers: chrX:g.153006349G>A (hg19) chrX:g.153740895G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740895G>A , CM000685.2:g.153740895G>A GRCh38
NC_000023.10:g.153006349G>A , CM000685.1:g.153006349G>A GRCh37
NC_000023.9:g.152659543G>A NCBI36
NG_009022.2:g.21028G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1780+176G>A MANE Select ENSP00000218104.3:n.1780+176G>A
ENST00000218104.5:c.1780+176G>A ENSP00000218104.3:n.1780+176G>A
NM_000033.3:c.1780+176G>A NP_000024.2:n.1780+176G>A
XR_938507.1:n.2252+176G>A
XR_938507.2:n.2252+176G>A
NM_000033.4:c.1780+176G>A MANE Select NP_000024.2:n.1780+176G>A
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