Canonical Allele Identifier: CA2602662098
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs2148397516

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740085C>T , CM000685.2:g.153740085C>T GRCh38
NC_000023.10:g.153005539C>T , CM000685.1:g.153005539C>T GRCh37
NC_000023.9:g.152658733C>T NCBI36
NG_009022.2:g.20218C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1489-7C>T MANE Select ENSP00000218104.3:n.1489-7C>T
ENST00000218104.5:c.1489-7C>T ENSP00000218104.3:n.1489-7C>T
ENST00000443684.2:n.492-7C>T
NM_000033.3:c.1489-7C>T NP_000024.2:n.1489-7C>T
XR_938507.1:n.1961-7C>T
XR_938507.2:n.1961-7C>T
NM_000033.4:c.1489-7C>T MANE Select NP_000024.2:n.1489-7C>T