Canonical Allele Identifier: CA1953603940
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1848922089

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076879C>T , CM000673.2:g.14076879C>T GRCh38
NC_000011.9:g.14098426C>T , CM000673.1:g.14098426C>T GRCh37
NC_000011.8:g.14055002C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.553+1461C>T MANE Select ENSP00000460236.1:n.553+1461C>T
ENST00000576479.3:c.553+1461C>T ENSP00000460236.1:n.553+1461C>T
NM_006108.3:c.553+1461C>T NP_006099.2:n.553+1461C>T
NM_006108.4:c.553+1461C>T MANE Select NP_006099.2:n.553+1461C>T