Canonical Allele Identifier: CA337242039
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs782252073

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