Canonical Allele Identifier: CA832638583
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1330534762

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234141A>C , CM000669.2:g.1234141A>C GRCh38
NC_000007.13:g.1273777A>C , CM000669.1:g.1273777A>C GRCh37
NC_000007.12:g.1240303A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+446A>C MANE Select ENSP00000314480.8:n.450+446A>C
ENST00000316333.8:c.450+446A>C ENSP00000314480.8:n.450+446A>C
NM_001080461.1:c.450+446A>C NP_001073930.1:n.450+446A>C
NM_001080461.2:c.450+446A>C NP_001073930.1:n.450+446A>C
NM_001080461.3:c.450+446A>C MANE Select NP_001073930.1:n.450+446A>C