Canonical Allele Identifier: CA218160264
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1018305156
MyVariant Identifiers: chr11:g.13974453A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13974453A>G , CM000673.2:g.13974453A>G GRCh38
NC_000011.9:g.13996000A>G , CM000673.1:g.13996000A>G GRCh37
NC_000011.8:g.13952576A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.239-8394A>G MANE Select ENSP00000460236.1:n.239-8394A>G
ENST00000576479.3:c.239-8394A>G ENSP00000460236.1:n.239-8394A>G
NM_006108.3:c.239-8394A>G NP_006099.2:n.239-8394A>G
NM_006108.4:c.239-8394A>G MANE Select NP_006099.2:n.239-8394A>G