Canonical Allele Identifier: CA1953603926
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1848921887
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076846A>T , CM000673.2:g.14076846A>T GRCh38
NC_000011.9:g.14098393A>T , CM000673.1:g.14098393A>T GRCh37
NC_000011.8:g.14054969A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.553+1428A>T MANE Select ENSP00000460236.1:n.553+1428A>T
ENST00000576479.3:c.553+1428A>T ENSP00000460236.1:n.553+1428A>T
NM_006108.3:c.553+1428A>T NP_006099.2:n.553+1428A>T
NM_006108.4:c.553+1428A>T MANE Select NP_006099.2:n.553+1428A>T
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