Canonical Allele Identifier: CA2578570634
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31859653-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859653T>C , CM000668.2:g.31859653T>C GRCh38
NC_000006.11:g.31827430T>C , CM000668.1:g.31827430T>C GRCh37
NC_000006.10:g.31935409T>C NCBI36
NG_008201.1:g.8280A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*66A>G MANE Select ENSP00000364782.4:n.*66A>G
ENST00000677054.1:n.2653A>G
ENST00000677512.1:n.1591A>G
ENST00000678869.1:n.1902A>G
ENST00000375631.4:c.*66A>G ENSP00000364782.4:n.*66A>G
ENST00000480384.1:n.1613A>G
ENST00000491768.5:c.*424A>G ENSP00000433127.1:n.*424A>G
ENST00000495807.1:n.2622A>G
NM_000434.3:c.*66A>G NP_000425.1:n.*66A>G
NM_000434.4:c.*66A>G MANE Select NP_000425.1:n.*66A>G
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