Canonical Allele Identifier: CA673918906
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1217384687
MyVariant Identifiers: chr11:g.14076890C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076890C>T , CM000673.2:g.14076890C>T GRCh38
NC_000011.9:g.14098437C>T , CM000673.1:g.14098437C>T GRCh37
NC_000011.8:g.14055013C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.553+1472C>T MANE Select ENSP00000460236.1:n.553+1472C>T
ENST00000576479.3:c.553+1472C>T ENSP00000460236.1:n.553+1472C>T
NM_006108.3:c.553+1472C>T NP_006099.2:n.553+1472C>T
NM_006108.4:c.553+1472C>T MANE Select NP_006099.2:n.553+1472C>T