Canonical Allele Identifier: CA1682451641
Gene: UNCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234177A= , CM000669.2:g.1234177A= GRCh38
NC_000007.13:g.1273813A= , CM000669.1:g.1273813A= GRCh37
NC_000007.12:g.1240339A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+482A= MANE Select ENSP00000314480.8:n.450+482A=
ENST00000316333.8:c.450+482A= ENSP00000314480.8:n.450+482A=
NM_001080461.1:c.450+482A= NP_001073930.1:n.450+482A=
NM_001080461.2:c.450+482A= NP_001073930.1:n.450+482A=
NM_001080461.3:c.450+482A= MANE Select NP_001073930.1:n.450+482A=
Search 100 bp 5'
Search 100 bp 3'