Canonical Allele Identifier: CA2260526565
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs1399880995

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536157A>C , CM000679.2:g.42536157A>C GRCh38
NC_000017.10:g.40688175A>C , CM000679.1:g.40688175A>C GRCh37
NC_000017.9:g.37941701A>C NCBI36
NG_011552.1:g.5225A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000263.3:c.-116A>C NP_000254.2:n.-116A>C
XM_024450771.1:c.-116A>C XP_024306539.1:n.-116A>C