Canonical Allele Identifier: CA500216162
Gene: NAGLU HGNC NCBI

Linked Data

gnomAD v4: 17-42536512-C-T
MyVariant Identifiers: chr17:g.40688530C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536512C>T , CM000679.2:g.42536512C>T GRCh38
NC_000017.10:g.40688530C>T , CM000679.1:g.40688530C>T GRCh37
NC_000017.9:g.37942056C>T NCBI36
NG_011552.1:g.5580C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.240C>T MANE Select ENSP00000225927.1:p.Ser80=
ENST00000225927.6:c.240C>T ENSP00000225927.1:p.Ser80=
NM_000263.3:c.240C>T NP_000254.2:p.Ser80=
XM_024450771.1:c.240C>T XP_024306539.1:p.Ser80=
NM_000263.4:c.240C>T MANE Select NP_000254.2:p.Ser80=
Search 100 bp 5'
Search 100 bp 3'