Canonical Allele Identifier: CA1682451566

Gene: UNCX

Linked Data

• dbSNP Id: rs1376787587

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234082C>A , CM000669.2:g.1234082C>A	GRCh38
NC_000007.13:g.1273718C>A , CM000669.1:g.1273718C>A	GRCh37
NC_000007.12:g.1240244C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+387C>A MANE Select	ENSP00000314480.8:n.450+387C>A
ENST00000316333.8:c.450+387C>A	ENSP00000314480.8:n.450+387C>A
NM_001080461.1:c.450+387C>A	NP_001073930.1:n.450+387C>A
NM_001080461.2:c.450+387C>A	NP_001073930.1:n.450+387C>A
NM_001080461.3:c.450+387C>A MANE Select	NP_001073930.1:n.450+387C>A