Canonical Allele Identifier: CA136925146
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs923866884
gnomAD v4: 6-31859637-C-A
MyVariant Identifiers: chr6:g.31859637C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859637C>A , CM000668.2:g.31859637C>A GRCh38
NC_000006.11:g.31827414C>A , CM000668.1:g.31827414C>A GRCh37
NC_000006.10:g.31935393C>A NCBI36
NG_008201.1:g.8296G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*82G>T MANE Select ENSP00000364782.4:n.*82G>T
ENST00000677054.1:n.2669G>T
ENST00000677512.1:n.1607G>T
ENST00000678869.1:n.1918G>T
ENST00000375631.4:c.*82G>T ENSP00000364782.4:n.*82G>T
ENST00000480384.1:n.1629G>T
ENST00000491768.5:c.*440G>T ENSP00000433127.1:n.*440G>T
ENST00000495807.1:n.2638G>T
NM_000434.3:c.*82G>T NP_000425.1:n.*82G>T
NM_000434.4:c.*82G>T MANE Select NP_000425.1:n.*82G>T
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