Canonical Allele Identifier: CA772108838
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs1168656848
gnomAD v3: 17-42536163-G-A
gnomAD v4: 17-42536163-G-A
MyVariant Identifiers: chr17:g.40688181G>A (hg19) chr17:g.42536163G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536163G>A , CM000679.2:g.42536163G>A GRCh38
NC_000017.10:g.40688181G>A , CM000679.1:g.40688181G>A GRCh37
NC_000017.9:g.37941707G>A NCBI36
NG_011552.1:g.5231G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000263.3:c.-110G>A NP_000254.2:n.-110G>A
XM_024450771.1:c.-110G>A XP_024306539.1:n.-110G>A
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