Canonical Allele Identifier: CA290771077
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs897736289
MyVariant Identifiers: chr17:g.42536240C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536240C>G , CM000679.2:g.42536240C>G GRCh38
NC_000017.10:g.40688258C>G , CM000679.1:g.40688258C>G GRCh37
NC_000017.9:g.37941784C>G NCBI36
NG_011552.1:g.5308C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.6:c.-33C>G ENSP00000225927.1:n.-33C>G
NM_000263.3:c.-33C>G NP_000254.2:n.-33C>G
XM_024450771.1:c.-33C>G XP_024306539.1:n.-33C>G