Canonical Allele Identifier: CA2260526569
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536162T= , CM000679.2:g.42536162T= GRCh38
NC_000017.10:g.40688180T= , CM000679.1:g.40688180T= GRCh37
NC_000017.9:g.37941706T= NCBI36
NG_011552.1:g.5230T=

Transcript Alleles

HGVS Amino-acid Change
NM_000263.3:c.-111T= NP_000254.2:n.-111T=
XM_024450771.1:c.-111T= XP_024306539.1:n.-111T=