Canonical Allele Identifier: CA152421741

Gene: UNCX

Linked Data

• dbSNP Id: rs929594490
• gnomAD v3: 7-1234178-T-A
• gnomAD v4: 7-1234178-T-A
• MyVariant Identifiers: chr7:g.1273814T>A (hg19) ; chr7:g.1234178T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234178T>A , CM000669.2:g.1234178T>A	GRCh38
NC_000007.13:g.1273814T>A , CM000669.1:g.1273814T>A	GRCh37
NC_000007.12:g.1240340T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+483T>A MANE Select	ENSP00000314480.8:n.450+483T>A
ENST00000316333.8:c.450+483T>A	ENSP00000314480.8:n.450+483T>A
NM_001080461.1:c.450+483T>A	NP_001073930.1:n.450+483T>A
NM_001080461.2:c.450+483T>A	NP_001073930.1:n.450+483T>A
NM_001080461.3:c.450+483T>A MANE Select	NP_001073930.1:n.450+483T>A