Canonical Allele Identifier: CA415099054
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs2091708025
gnomAD v3: X-153725799-A-G
gnomAD v4: X-153725799-A-G
MyVariant Identifiers: chrX:g.152991254A>G (hg19) chrX:g.153725799A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153725799A>G , CM000685.2:g.153725799A>G GRCh38
NC_000023.10:g.152991254A>G , CM000685.1:g.152991254A>G GRCh37
NC_000023.9:g.152644448A>G NCBI36
NG_009022.2:g.5932A>G
NG_023231.1:g.3948T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.533A>G MANE Select ENSP00000218104.3:p.Gln178Arg
ENST00000218104.5:c.533A>G ENSP00000218104.3:p.Gln178Arg
NM_000033.3:c.533A>G NP_000024.2:p.Gln178Arg
XR_938507.1:n.949A>G
XR_938507.2:n.949A>G
NM_000033.4:c.533A>G MANE Select NP_000024.2:p.Gln178Arg
Search 100 bp 5'
Search 100 bp 3'