Canonical Allele Identifier: CA2260526639
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs2092905459
gnomAD v4: 17-42536250-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536250G>C , CM000679.2:g.42536250G>C GRCh38
NC_000017.10:g.40688268G>C , CM000679.1:g.40688268G>C GRCh37
NC_000017.9:g.37941794G>C NCBI36
NG_011552.1:g.5318G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-23G>C MANE Select ENSP00000225927.1:n.-23G>C
ENST00000225927.6:c.-23G>C ENSP00000225927.1:n.-23G>C
NM_000263.3:c.-23G>C NP_000254.2:n.-23G>C
XM_024450771.1:c.-23G>C XP_024306539.1:n.-23G>C
NM_000263.4:c.-23G>C MANE Select NP_000254.2:n.-23G>C
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