Linked Data
dbSNP Id:
rs372867684
gnomAD v2:
13-25457289-G-C
gnomAD v4:
13-24883151-G-C
MyVariant Identifiers:
chr13:g.25457289G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.24883151G>C , CM000675.2:g.24883151G>C | GRCh38 |
| NC_000013.10:g.25457289G>C , CM000675.1:g.25457289G>C | GRCh37 |
| NC_000013.9:g.24355289G>C | NCBI36 |
| NG_009165.2:g.44797C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381884.9:c.*26C>G (CENPJ) MANE Select | ENSP00000371308.4:n.*26C>G | |
| ENST00000381884.8:c.*26C>G (CENPJ) | ENSP00000371308.4:n.*26C>G | |
| ENST00000616936.4:c.*697C>G (CENPJ) | ENSP00000477511.1:n.*697C>G | |
| NM_018451.4:c.*26C>G (CENPJ) | NP_060921.3:n.*26C>G | |
| NR_047594.1:n.4355C>G (CENPJ) | ||
| NR_047595.1:n.4153C>G (CENPJ) | ||
| XM_011535156.1:c.*10+3856G>C (RNF17) | XP_011533458.1:n.*10+3856G>C | |
| XM_011535156.2:c.*10+3856G>C (RNF17) | XP_011533458.1:n.*10+3856G>C | |
| NM_018451.5:c.*26C>G (CENPJ) MANE Select | NP_060921.3:n.*26C>G | |
| NR_047594.2:n.4327C>G (CENPJ) | ||
| NR_047595.2:n.4125C>G (CENPJ) |