Canonical Allele Identifier: CA572109206
Gene: UNCX HGNC NCBI

Linked Data

gnomAD v2: 7-1273738-A-C
gnomAD v3: 7-1234102-A-C
gnomAD v4: 7-1234102-A-C
MyVariant Identifiers: chr7:g.1273738A>C (hg19) chr7:g.1234102A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234102A>C , CM000669.2:g.1234102A>C GRCh38
NC_000007.13:g.1273738A>C , CM000669.1:g.1273738A>C GRCh37
NC_000007.12:g.1240264A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+407A>C MANE Select ENSP00000314480.8:n.450+407A>C
ENST00000316333.8:c.450+407A>C ENSP00000314480.8:n.450+407A>C
NM_001080461.1:c.450+407A>C NP_001073930.1:n.450+407A>C
NM_001080461.2:c.450+407A>C NP_001073930.1:n.450+407A>C
NM_001080461.3:c.450+407A>C MANE Select NP_001073930.1:n.450+407A>C
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