Canonical Allele Identifier: CA873267508
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1376246228
MyVariant Identifiers: chrX:g.153736837G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736837G>T , CM000685.2:g.153736837G>T GRCh38
NC_000023.10:g.153002291G>T , CM000685.1:g.153002291G>T GRCh37
NC_000023.9:g.152655485G>T NCBI36
NG_009022.2:g.16970G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1394-320G>T MANE Select ENSP00000218104.3:n.1394-320G>T
ENST00000218104.5:c.1394-320G>T ENSP00000218104.3:n.1394-320G>T
ENST00000443684.2:n.397-320G>T
NM_000033.3:c.1394-320G>T NP_000024.2:n.1394-320G>T
XR_938507.1:n.1810-19G>T
XR_938507.2:n.1810-19G>T
NM_000033.4:c.1394-320G>T MANE Select NP_000024.2:n.1394-320G>T
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