Canonical Allele Identifier: CA1953603949
Gene: SPON1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076898G= , CM000673.2:g.14076898G= GRCh38
NC_000011.9:g.14098445G= , CM000673.1:g.14098445G= GRCh37
NC_000011.8:g.14055021G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.553+1480G= MANE Select ENSP00000460236.1:n.553+1480G=
ENST00000576479.3:c.553+1480G= ENSP00000460236.1:n.553+1480G=
NM_006108.3:c.553+1480G= NP_006099.2:n.553+1480G=
NM_006108.4:c.553+1480G= MANE Select NP_006099.2:n.553+1480G=
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