Canonical Allele Identifier: CA449808590
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31861383-C-T
MyVariant Identifiers: chr6:g.31829160C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861383C>T , CM000668.2:g.31861383C>T GRCh38
NC_000006.11:g.31829160C>T , CM000668.1:g.31829160C>T GRCh37
NC_000006.10:g.31937139C>T NCBI36
NG_008201.1:g.6550G>A
NG_023058.1:g.22664G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.420G>A MANE Select ENSP00000364782.4:p.Gly140=
ENST00000677054.1:n.1097G>A
ENST00000677512.1:n.528G>A
ENST00000678869.1:n.528G>A
ENST00000375631.4:c.420G>A ENSP00000364782.4:p.Gly140=
ENST00000480384.1:n.449G>A
ENST00000491768.5:c.420G>A ENSP00000433127.1:p.Gly140=
ENST00000495807.1:n.988G>A
NM_000434.3:c.420G>A NP_000425.1:p.Gly140=
NM_000434.4:c.420G>A MANE Select NP_000425.1:p.Gly140=
Search 100 bp 5'
Search 100 bp 3'