Linked Data
ClinVar Variation Id:
13870
ClinVar RCV Id:
RCV000014884
dbSNP Id:
rs267606828
PubMed:
PMID:19578037
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767922T>C , CM000676.2:g.28767922T>C | GRCh38 |
| NC_000014.8:g.29237128T>C , CM000676.1:g.29237128T>C | GRCh37 |
| NC_000014.7:g.28306879T>C | NCBI36 |
| NG_009367.1:g.5842T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000706482.1:c.643T>C | ENSP00000516406.1:p.Phe215Leu | |
| ENST00000313071.7:c.643T>C MANE Select | ENSP00000339004.3:p.Phe215Leu | |
| ENST00000313071.6:c.643T>C | ENSP00000339004.3:p.Phe215Leu | |
| NM_005249.4:c.643T>C | NP_005240.3:p.Phe215Leu | |
| NM_005249.5:c.643T>C MANE Select | NP_005240.3:p.Phe215Leu |