Canonical Allele Identifier: CA1953569736
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1848304895
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14000039G>A , CM000673.2:g.14000039G>A GRCh38
NC_000011.9:g.14021586G>A , CM000673.1:g.14021586G>A GRCh37
NC_000011.8:g.13978162G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.345+17086G>A MANE Select ENSP00000460236.1:n.345+17086G>A
ENST00000576479.3:c.345+17086G>A ENSP00000460236.1:n.345+17086G>A
NM_006108.3:c.345+17086G>A NP_006099.2:n.345+17086G>A
NM_006108.4:c.345+17086G>A MANE Select NP_006099.2:n.345+17086G>A
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