Canonical Allele Identifier: CA1953569738
Gene: SPON1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14000053A= , CM000673.2:g.14000053A= GRCh38
NC_000011.9:g.14021600A= , CM000673.1:g.14021600A= GRCh37
NC_000011.8:g.13978176A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.345+17100A= MANE Select ENSP00000460236.1:n.345+17100A=
ENST00000576479.3:c.345+17100A= ENSP00000460236.1:n.345+17100A=
NM_006108.3:c.345+17100A= NP_006099.2:n.345+17100A=
NM_006108.4:c.345+17100A= MANE Select NP_006099.2:n.345+17100A=