Canonical Allele Identifier: CA1181573502
Gene: ABCD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94418428G= , CM000663.2:g.94418428G= GRCh38
NC_000001.10:g.94883984G= , CM000663.1:g.94883984G= GRCh37
NC_000001.9:g.94656572G= NCBI36
NG_008865.1:g.5052G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370214.9:c.-51G= MANE Select ENSP00000359233.4:n.-51G=
NM_001122674.1:c.-51G= NP_001116146.1:n.-51G=
NM_002858.3:c.-51G= NP_002849.1:n.-51G=
XM_006710802.2:c.-51G= XP_006710865.2:n.-51G=
NM_002858.4:c.-51G= MANE Select NP_002849.1:n.-51G=
NM_001122674.2:c.-51G= NP_001116146.1:n.-51G=