Canonical Allele Identifier: CA218162455
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1011436241
MyVariant Identifiers: chr11:g.14000060A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14000060A>C , CM000673.2:g.14000060A>C GRCh38
NC_000011.9:g.14021607A>C , CM000673.1:g.14021607A>C GRCh37
NC_000011.8:g.13978183A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.345+17107A>C MANE Select ENSP00000460236.1:n.345+17107A>C
ENST00000576479.3:c.345+17107A>C ENSP00000460236.1:n.345+17107A>C
NM_006108.3:c.345+17107A>C NP_006099.2:n.345+17107A>C
NM_006108.4:c.345+17107A>C MANE Select NP_006099.2:n.345+17107A>C
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