Canonical Allele Identifier: CA832638581

Gene: UNCX

Linked Data

• dbSNP Id: rs1330534762
• MyVariant Identifiers: chr7:g.1273777A>G (hg19) ; chr7:g.1234141A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234141A>G , CM000669.2:g.1234141A>G	GRCh38
NC_000007.13:g.1273777A>G , CM000669.1:g.1273777A>G	GRCh37
NC_000007.12:g.1240303A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+446A>G MANE Select	ENSP00000314480.8:n.450+446A>G
ENST00000316333.8:c.450+446A>G	ENSP00000314480.8:n.450+446A>G
NM_001080461.1:c.450+446A>G	NP_001073930.1:n.450+446A>G
NM_001080461.2:c.450+446A>G	NP_001073930.1:n.450+446A>G
NM_001080461.3:c.450+446A>G MANE Select	NP_001073930.1:n.450+446A>G