Canonical Allele Identifier: CA1682451508
Gene: UNCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234022G= , CM000669.2:g.1234022G= GRCh38
NC_000007.13:g.1273658G= , CM000669.1:g.1273658G= GRCh37
NC_000007.12:g.1240184G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+327G= MANE Select ENSP00000314480.8:n.450+327G=
ENST00000316333.8:c.450+327G= ENSP00000314480.8:n.450+327G=
NM_001080461.1:c.450+327G= NP_001073930.1:n.450+327G=
NM_001080461.2:c.450+327G= NP_001073930.1:n.450+327G=
NM_001080461.3:c.450+327G= MANE Select NP_001073930.1:n.450+327G=
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