Canonical Allele Identifier: CA983827475
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs1402396195
gnomAD v3: 17-42536231-G-C
gnomAD v4: 17-42536231-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536231G>C , CM000679.2:g.42536231G>C GRCh38
NC_000017.10:g.40688249G>C , CM000679.1:g.40688249G>C GRCh37
NC_000017.9:g.37941775G>C NCBI36
NG_011552.1:g.5299G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225927.6:c.-42G>C ENSP00000225927.1:n.-42G>C
NM_000263.3:c.-42G>C NP_000254.2:n.-42G>C
XM_024450771.1:c.-42G>C XP_024306539.1:n.-42G>C
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