Canonical Allele Identifier: CA399595542
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs2092906317

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536453G>A , CM000679.2:g.42536453G>A GRCh38
NC_000017.10:g.40688471G>A , CM000679.1:g.40688471G>A GRCh37
NC_000017.9:g.37941997G>A NCBI36
NG_011552.1:g.5521G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.181G>A MANE Select ENSP00000225927.1:p.Gly61Ser
ENST00000225927.6:c.181G>A ENSP00000225927.1:p.Gly61Ser
NM_000263.3:c.181G>A NP_000254.2:p.Gly61Ser
XM_024450771.1:c.181G>A XP_024306539.1:p.Gly61Ser
NM_000263.4:c.181G>A MANE Select NP_000254.2:p.Gly61Ser