Canonical Allele Identifier: CA418833666
Gene: ABCD3 HGNC NCBI

Linked Data

gnomAD v4: 1-94418541-G-T
MyVariant Identifiers: chr1:g.94884097G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94418541G>T , CM000663.2:g.94418541G>T GRCh38
NC_000001.10:g.94884097G>T , CM000663.1:g.94884097G>T GRCh37
NC_000001.9:g.94656685G>T NCBI36
NG_008865.1:g.5165G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370214.9:c.63G>T MANE Select ENSP00000359233.4:p.Leu21=
ENST00000647998.2:c.63G>T ENSP00000497921.2:p.Leu21=
ENST00000315713.5:c.63G>T ENSP00000326880.5:p.Leu21=
ENST00000370214.8:c.63G>T ENSP00000359233.4:p.Leu21=
NM_001122674.1:c.63G>T NP_001116146.1:p.Leu21=
NM_002858.3:c.63G>T NP_002849.1:p.Leu21=
XM_006710802.2:c.63G>T XP_006710865.2:p.Leu21=
NM_002858.4:c.63G>T MANE Select NP_002849.1:p.Leu21=
NM_001122674.2:c.63G>T NP_001116146.1:p.Leu21=