Canonical Allele Identifier: CA2260526598
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536207C= , CM000679.2:g.42536207C= GRCh38
NC_000017.10:g.40688225C= , CM000679.1:g.40688225C= GRCh37
NC_000017.9:g.37941751C= NCBI36
NG_011552.1:g.5275C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.6:c.-66C= ENSP00000225927.1:n.-66C=
NM_000263.3:c.-66C= NP_000254.2:n.-66C=
XM_024450771.1:c.-66C= XP_024306539.1:n.-66C=