Canonical Allele Identifier: CA152421809

Gene: UNCX

Linked Data

• dbSNP Id: rs188618554
• gnomAD v2: 7-1273914-A-G
• gnomAD v3: 7-1234278-A-G
• gnomAD v4: 7-1234278-A-G
• MyVariant Identifiers: chr7:g.1273914A>G (hg19) ; chr7:g.1234278A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234278A>G , CM000669.2:g.1234278A>G	GRCh38
NC_000007.13:g.1273914A>G , CM000669.1:g.1273914A>G	GRCh37
NC_000007.12:g.1240440A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+583A>G MANE Select	ENSP00000314480.8:n.450+583A>G
ENST00000316333.8:c.450+583A>G	ENSP00000314480.8:n.450+583A>G
NM_001080461.1:c.450+583A>G	NP_001073930.1:n.450+583A>G
NM_001080461.2:c.450+583A>G	NP_001073930.1:n.450+583A>G
NM_001080461.3:c.450+583A>G MANE Select	NP_001073930.1:n.450+583A>G