Canonical Allele Identifier: CA1682451736

Gene: UNCX

Linked Data

• dbSNP Id: rs1778703496

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234360T>C , CM000669.2:g.1234360T>C	GRCh38
NC_000007.13:g.1273996T>C , CM000669.1:g.1273996T>C	GRCh37
NC_000007.12:g.1240522T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+665T>C MANE Select	ENSP00000314480.8:n.450+665T>C
ENST00000316333.8:c.450+665T>C	ENSP00000314480.8:n.450+665T>C
NM_001080461.1:c.450+665T>C	NP_001073930.1:n.450+665T>C
NM_001080461.2:c.450+665T>C	NP_001073930.1:n.450+665T>C
NM_001080461.3:c.450+665T>C MANE Select	NP_001073930.1:n.450+665T>C