Canonical Allele Identifier: CA2260526621
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs2092905386

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536236A>C , CM000679.2:g.42536236A>C GRCh38
NC_000017.10:g.40688254A>C , CM000679.1:g.40688254A>C GRCh37
NC_000017.9:g.37941780A>C NCBI36
NG_011552.1:g.5304A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.6:c.-37A>C ENSP00000225927.1:n.-37A>C
NM_000263.3:c.-37A>C NP_000254.2:n.-37A>C
XM_024450771.1:c.-37A>C XP_024306539.1:n.-37A>C