Canonical Allele Identifier: CA152421846

Gene: UNCX

Linked Data

• dbSNP Id: rs1022785771
• gnomAD v2: 7-1273998-G-A
• gnomAD v3: 7-1234362-G-A
• gnomAD v4: 7-1234362-G-A
• MyVariant Identifiers: chr7:g.1273998G>A (hg19) ; chr7:g.1234362G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234362G>A , CM000669.2:g.1234362G>A	GRCh38
NC_000007.13:g.1273998G>A , CM000669.1:g.1273998G>A	GRCh37
NC_000007.12:g.1240524G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+667G>A MANE Select	ENSP00000314480.8:n.450+667G>A
ENST00000316333.8:c.450+667G>A	ENSP00000314480.8:n.450+667G>A
NM_001080461.1:c.450+667G>A	NP_001073930.1:n.450+667G>A
NM_001080461.2:c.450+667G>A	NP_001073930.1:n.450+667G>A
NM_001080461.3:c.450+667G>A MANE Select	NP_001073930.1:n.450+667G>A