Canonical Allele Identifier: CA26875961
Gene: ABCD3 HGNC NCBI

Linked Data

dbSNP Id: rs532074242
gnomAD v3: 1-94418535-G-T
gnomAD v4: 1-94418535-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94418535G>T , CM000663.2:g.94418535G>T GRCh38
NC_000001.10:g.94884091G>T , CM000663.1:g.94884091G>T GRCh37
NC_000001.9:g.94656679G>T NCBI36
NG_008865.1:g.5159G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370214.9:c.57G>T MANE Select ENSP00000359233.4:p.Ala19=
ENST00000647998.2:c.57G>T ENSP00000497921.2:p.Ala19=
ENST00000315713.5:c.57G>T ENSP00000326880.5:p.Ala19=
ENST00000370214.8:c.57G>T ENSP00000359233.4:p.Ala19=
NM_001122674.1:c.57G>T NP_001116146.1:p.Ala19=
NM_002858.3:c.57G>T NP_002849.1:p.Ala19=
XM_006710802.2:c.57G>T XP_006710865.2:p.Ala19=
NM_002858.4:c.57G>T MANE Select NP_002849.1:p.Ala19=
NM_001122674.2:c.57G>T NP_001116146.1:p.Ala19=