Canonical Allele Identifier: CA2260526634
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs987583207
gnomAD v4: 17-42536246-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536246C>T , CM000679.2:g.42536246C>T GRCh38
NC_000017.10:g.40688264C>T , CM000679.1:g.40688264C>T GRCh37
NC_000017.9:g.37941790C>T NCBI36
NG_011552.1:g.5314C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-27C>T MANE Select ENSP00000225927.1:n.-27C>T
ENST00000225927.6:c.-27C>T ENSP00000225927.1:n.-27C>T
NM_000263.3:c.-27C>T NP_000254.2:n.-27C>T
XM_024450771.1:c.-27C>T XP_024306539.1:n.-27C>T
NM_000263.4:c.-27C>T MANE Select NP_000254.2:n.-27C>T
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