Canonical Allele Identifier: CA1682451589
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1169257838

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234103A>T , CM000669.2:g.1234103A>T GRCh38
NC_000007.13:g.1273739A>T , CM000669.1:g.1273739A>T GRCh37
NC_000007.12:g.1240265A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+408A>T MANE Select ENSP00000314480.8:n.450+408A>T
ENST00000316333.8:c.450+408A>T ENSP00000314480.8:n.450+408A>T
NM_001080461.1:c.450+408A>T NP_001073930.1:n.450+408A>T
NM_001080461.2:c.450+408A>T NP_001073930.1:n.450+408A>T
NM_001080461.3:c.450+408A>T MANE Select NP_001073930.1:n.450+408A>T