Canonical Allele Identifier: CA363486755
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31827829A>C (hg19) chr6:g.31860052A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860052A>C , CM000668.2:g.31860052A>C GRCh38
NC_000006.11:g.31827829A>C , CM000668.1:g.31827829A>C GRCh37
NC_000006.10:g.31935808A>C NCBI36
NG_008201.1:g.7881T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.1011T>G MANE Select ENSP00000364782.4:p.His337Gln
ENST00000677054.1:n.2254T>G
ENST00000677512.1:n.1293T>G
ENST00000678869.1:n.1599T>G
ENST00000375631.4:c.1011T>G ENSP00000364782.4:p.His337Gln
ENST00000480384.1:n.1214T>G
ENST00000491768.5:c.*121T>G ENSP00000433127.1:n.*121T>G
ENST00000495807.1:n.2319T>G
NM_000434.3:c.1011T>G NP_000425.1:p.His337Gln
NM_000434.4:c.1011T>G MANE Select NP_000425.1:p.His337Gln
Search 100 bp 5'
Search 100 bp 3'