Canonical Allele Identifier: CA597787698
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1554921513

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076891C>T , CM000673.2:g.14076891C>T GRCh38
NC_000011.9:g.14098438C>T , CM000673.1:g.14098438C>T GRCh37
NC_000011.8:g.14055014C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.553+1473C>T MANE Select ENSP00000460236.1:n.553+1473C>T
ENST00000576479.3:c.553+1473C>T ENSP00000460236.1:n.553+1473C>T
NM_006108.3:c.553+1473C>T NP_006099.2:n.553+1473C>T
NM_006108.4:c.553+1473C>T MANE Select NP_006099.2:n.553+1473C>T