Canonical Allele Identifier: CA873267473
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1197133978
MyVariant Identifiers: chrX:g.153736740G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736740G>T , CM000685.2:g.153736740G>T GRCh38
NC_000023.10:g.153002194G>T , CM000685.1:g.153002194G>T GRCh37
NC_000023.9:g.152655388G>T NCBI36
NG_009022.2:g.16873G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1393+227G>T MANE Select ENSP00000218104.3:n.1393+227G>T
ENST00000218104.5:c.1393+227G>T ENSP00000218104.3:n.1393+227G>T
ENST00000443684.2:n.396+227G>T
NM_000033.3:c.1393+227G>T NP_000024.2:n.1393+227G>T
XR_938507.1:n.1810-116G>T
XR_938507.2:n.1810-116G>T
NM_000033.4:c.1393+227G>T MANE Select NP_000024.2:n.1393+227G>T
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Search 100 bp 3'