Canonical Allele Identifier: CA1953569725
Gene: SPON1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14000020T= , CM000673.2:g.14000020T= GRCh38
NC_000011.9:g.14021567T= , CM000673.1:g.14021567T= GRCh37
NC_000011.8:g.13978143T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.345+17067T= MANE Select ENSP00000460236.1:n.345+17067T=
ENST00000576479.3:c.345+17067T= ENSP00000460236.1:n.345+17067T=
NM_006108.3:c.345+17067T= NP_006099.2:n.345+17067T=
NM_006108.4:c.345+17067T= MANE Select NP_006099.2:n.345+17067T=
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