Canonical Allele Identifier: CA418833616
Gene: ABCD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2725974
ClinVar RCV Id: RCV003554747
dbSNP Id: rs749980366
gnomAD v2: 1-94884088-C-T
gnomAD v3: 1-94418532-C-T
gnomAD v4: 1-94418532-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94418532C>T , CM000663.2:g.94418532C>T GRCh38
NC_000001.10:g.94884088C>T , CM000663.1:g.94884088C>T GRCh37
NC_000001.9:g.94656676C>T NCBI36
NG_008865.1:g.5156C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370214.9:c.54C>T MANE Select ENSP00000359233.4:p.Ala18=
ENST00000647998.2:c.54C>T ENSP00000497921.2:p.Ala18=
ENST00000315713.5:c.54C>T ENSP00000326880.5:p.Ala18=
ENST00000370214.8:c.54C>T ENSP00000359233.4:p.Ala18=
NM_001122674.1:c.54C>T NP_001116146.1:p.Ala18=
NM_002858.3:c.54C>T NP_002849.1:p.Ala18=
XM_006710802.2:c.54C>T XP_006710865.2:p.Ala18=
NM_002858.4:c.54C>T MANE Select NP_002849.1:p.Ala18=
NM_001122674.2:c.54C>T NP_001116146.1:p.Ala18=