Canonical Allele Identifier: CA3725043
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs775901208
ExAC: 6:31829226 G / T
gnomAD v2: 6-31829226-G-T
gnomAD v4: 6-31861449-G-T
MyVariant Identifiers: chr6:g.31829226G>T (hg19) chr6:g.31861449G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861449G>T , CM000668.2:g.31861449G>T GRCh38
NC_000006.11:g.31829226G>T , CM000668.1:g.31829226G>T GRCh37
NC_000006.10:g.31937205G>T NCBI36
NG_008201.1:g.6484C>A
NG_023058.1:g.22598C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.354C>A MANE Select ENSP00000364782.4:p.Gly118=
ENST00000677054.1:n.1031C>A
ENST00000677512.1:n.462C>A
ENST00000678869.1:n.462C>A
ENST00000375631.4:c.354C>A ENSP00000364782.4:p.Gly118=
ENST00000480384.1:n.383C>A
ENST00000491768.5:c.354C>A ENSP00000433127.1:p.Gly118=
ENST00000495807.1:n.922C>A
NM_000434.3:c.354C>A NP_000425.1:p.Gly118=
NM_000434.4:c.354C>A MANE Select NP_000425.1:p.Gly118=
Search 100 bp 5'
Search 100 bp 3'