Canonical Allele Identifier: CA136927195
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs766029281
MyVariant Identifiers: chr6:g.31829293G>T (hg19) chr6:g.31861516G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861516G>T , CM000668.2:g.31861516G>T GRCh38
NC_000006.11:g.31829293G>T , CM000668.1:g.31829293G>T GRCh37
NC_000006.10:g.31937272G>T NCBI36
NG_008201.1:g.6417C>A
NG_023058.1:g.22531C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-66C>A MANE Select ENSP00000364782.4:n.353-66C>A
ENST00000677054.1:n.964C>A
ENST00000677512.1:n.461-66C>A
ENST00000678869.1:n.461-66C>A
ENST00000375631.4:c.353-66C>A ENSP00000364782.4:n.353-66C>A
ENST00000480384.1:n.382-66C>A
ENST00000491768.5:c.353-66C>A ENSP00000433127.1:n.353-66C>A
ENST00000495807.1:n.855C>A
NM_000434.3:c.353-66C>A NP_000425.1:n.353-66C>A
NM_000434.4:c.353-66C>A MANE Select NP_000425.1:n.353-66C>A
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