Canonical Allele Identifier: CA2260526594
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536202G= , CM000679.2:g.42536202G= GRCh38
NC_000017.10:g.40688220G= , CM000679.1:g.40688220G= GRCh37
NC_000017.9:g.37941746G= NCBI36
NG_011552.1:g.5270G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.6:c.-71G= ENSP00000225927.1:n.-71G=
NM_000263.3:c.-71G= NP_000254.2:n.-71G=
XM_024450771.1:c.-71G= XP_024306539.1:n.-71G=