Linked Data
ClinVar Variation Id:
15815
ClinVar RCV Id:
RCV000017157
dbSNP Id:
rs33935328
gnomAD v4:
16-177407-G-C
PubMed:
PMID:5782115
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177407G>C , CM000678.2:g.177407G>C | GRCh38 |
| NC_000016.9:g.227406G>C , CM000678.1:g.227406G>C | GRCh37 |
| NC_000016.8:g.167406G>C | NCBI36 |
| NG_000006.1:g.38270G>C | |
| NG_059186.1:g.5757G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320868.9:c.425G>C MANE Select | ENSP00000322421.5:p.Arg142Pro | |
| ENST00000397797.1:c.329G>C | ENSP00000380899.1:p.Arg110Pro | |
| ENST00000472694.1:n.561G>C | ||
| NM_000558.4:c.425G>C | NP_000549.1:p.Arg142Pro | |
| NM_000558.5:c.425G>C MANE Select | NP_000549.1:p.Arg142Pro |