Canonical Allele Identifier: CA449808229
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31828258A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860481A>G , CM000668.2:g.31860481A>G GRCh38
NC_000006.11:g.31828258A>G , CM000668.1:g.31828258A>G GRCh37
NC_000006.10:g.31936237A>G NCBI36
NG_008201.1:g.7452T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.756T>C MANE Select ENSP00000364782.4:p.Gly252=
ENST00000677054.1:n.1999T>C
ENST00000677512.1:n.864T>C
ENST00000678869.1:n.1430T>C
ENST00000375631.4:c.756T>C ENSP00000364782.4:p.Gly252=
ENST00000480384.1:n.785T>C
ENST00000491768.5:c.756T>C ENSP00000433127.1:p.Gly252=
ENST00000495807.1:n.1890T>C
NM_000434.3:c.756T>C NP_000425.1:p.Gly252=
NM_000434.4:c.756T>C MANE Select NP_000425.1:p.Gly252=
Search 100 bp 5'
Search 100 bp 3'