Canonical Allele Identifier: CA673918877
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1475799283
MyVariant Identifiers: chr11:g.14076860G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076860G>C , CM000673.2:g.14076860G>C GRCh38
NC_000011.9:g.14098407G>C , CM000673.1:g.14098407G>C GRCh37
NC_000011.8:g.14054983G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.553+1442G>C MANE Select ENSP00000460236.1:n.553+1442G>C
ENST00000576479.3:c.553+1442G>C ENSP00000460236.1:n.553+1442G>C
NM_006108.3:c.553+1442G>C NP_006099.2:n.553+1442G>C
NM_006108.4:c.553+1442G>C MANE Select NP_006099.2:n.553+1442G>C