Canonical Allele Identifier: CA935275832
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1848922267

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076903C>G , CM000673.2:g.14076903C>G GRCh38
NC_000011.9:g.14098450C>G , CM000673.1:g.14098450C>G GRCh37
NC_000011.8:g.14055026C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.553+1485C>G MANE Select ENSP00000460236.1:n.553+1485C>G
ENST00000576479.3:c.553+1485C>G ENSP00000460236.1:n.553+1485C>G
NM_006108.3:c.553+1485C>G NP_006099.2:n.553+1485C>G
NM_006108.4:c.553+1485C>G MANE Select NP_006099.2:n.553+1485C>G