Canonical Allele Identifier: CA1682451516

Gene: UNCX

Linked Data

• dbSNP Id: rs1778693611

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234030G>A , CM000669.2:g.1234030G>A	GRCh38
NC_000007.13:g.1273666G>A , CM000669.1:g.1273666G>A	GRCh37
NC_000007.12:g.1240192G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+335G>A MANE Select	ENSP00000314480.8:n.450+335G>A
ENST00000316333.8:c.450+335G>A	ENSP00000314480.8:n.450+335G>A
NM_001080461.1:c.450+335G>A	NP_001073930.1:n.450+335G>A
NM_001080461.2:c.450+335G>A	NP_001073930.1:n.450+335G>A
NM_001080461.3:c.450+335G>A MANE Select	NP_001073930.1:n.450+335G>A