Canonical Allele Identifier: CA1682451581
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1308824469

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234094A>G , CM000669.2:g.1234094A>G GRCh38
NC_000007.13:g.1273730A>G , CM000669.1:g.1273730A>G GRCh37
NC_000007.12:g.1240256A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+399A>G MANE Select ENSP00000314480.8:n.450+399A>G
ENST00000316333.8:c.450+399A>G ENSP00000314480.8:n.450+399A>G
NM_001080461.1:c.450+399A>G NP_001073930.1:n.450+399A>G
NM_001080461.2:c.450+399A>G NP_001073930.1:n.450+399A>G
NM_001080461.3:c.450+399A>G MANE Select NP_001073930.1:n.450+399A>G