Canonical Allele Identifier: CA1953569730
Gene: SPON1 HGNC NCBI

Linked Data

dbSNP Id: rs1564882963
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14000027C>T , CM000673.2:g.14000027C>T GRCh38
NC_000011.9:g.14021574C>T , CM000673.1:g.14021574C>T GRCh37
NC_000011.8:g.13978150C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000576479.4:c.345+17074C>T MANE Select ENSP00000460236.1:n.345+17074C>T
ENST00000576479.3:c.345+17074C>T ENSP00000460236.1:n.345+17074C>T
NM_006108.3:c.345+17074C>T NP_006099.2:n.345+17074C>T
NM_006108.4:c.345+17074C>T MANE Select NP_006099.2:n.345+17074C>T
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