Canonical Allele Identifier: CA415115596
Gene: ABCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2690501
ClinVar RCV Id: RCV003491879
gnomAD v4: X-153742986-G-T
MyVariant Identifiers: chrX:g.153008440G>T (hg19) chrX:g.153742986G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742986G>T , CM000685.2:g.153742986G>T GRCh38
NC_000023.10:g.153008440G>T , CM000685.1:g.153008440G>T GRCh37
NC_000023.9:g.152661634G>T NCBI36
NG_009022.2:g.23119G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1781-1G>T MANE Select ENSP00000218104.3:n.1781-1G>T
ENST00000218104.5:c.1781-1G>T ENSP00000218104.3:n.1781-1G>T
NM_000033.3:c.1781-1G>T NP_000024.2:n.1781-1G>T
XR_938507.1:n.2253-1G>T
XR_938507.2:n.2253-1G>T
NM_000033.4:c.1781-1G>T MANE Select NP_000024.2:n.1781-1G>T
Search 100 bp 5'
Search 100 bp 3'