Canonical Allele Identifier: CA673914439
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1281463459
MyVariant Identifiers: chr11:g.13974699T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13974699T>A , CM000673.2:g.13974699T>A GRCh38
NC_000011.9:g.13996246T>A , CM000673.1:g.13996246T>A GRCh37
NC_000011.8:g.13952822T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.239-8148T>A MANE Select ENSP00000460236.1:n.239-8148T>A
ENST00000576479.3:c.239-8148T>A ENSP00000460236.1:n.239-8148T>A
NM_006108.3:c.239-8148T>A NP_006099.2:n.239-8148T>A
NM_006108.4:c.239-8148T>A MANE Select NP_006099.2:n.239-8148T>A