Canonical Allele Identifier: CA363487989
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31827906C>G (hg19) chr6:g.31860129C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860129C>G , CM000668.2:g.31860129C>G GRCh38
NC_000006.11:g.31827906C>G , CM000668.1:g.31827906C>G GRCh37
NC_000006.10:g.31935885C>G NCBI36
NG_008201.1:g.7804G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.934G>C MANE Select ENSP00000364782.4:p.Glu312Gln
ENST00000677054.1:n.2177G>C
ENST00000677512.1:n.1216G>C
ENST00000678869.1:n.1522G>C
ENST00000375631.4:c.934G>C ENSP00000364782.4:p.Glu312Gln
ENST00000480384.1:n.1137G>C
ENST00000491768.5:c.*44G>C ENSP00000433127.1:n.*44G>C
ENST00000495807.1:n.2242G>C
NM_000434.3:c.934G>C NP_000425.1:p.Glu312Gln
NM_000434.4:c.934G>C MANE Select NP_000425.1:p.Glu312Gln
Search 100 bp 5'
Search 100 bp 3'