Canonical Allele Identifier: CA2260526568
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536161C= , CM000679.2:g.42536161C= GRCh38
NC_000017.10:g.40688179C= , CM000679.1:g.40688179C= GRCh37
NC_000017.9:g.37941705C= NCBI36
NG_011552.1:g.5229C=

Transcript Alleles

HGVS Amino-acid Change
NM_000263.3:c.-112C= NP_000254.2:n.-112C=
XM_024450771.1:c.-112C= XP_024306539.1:n.-112C=