Linked Data
ClinVar Variation Id:
16009
dbSNP Id:
rs63750331
gnomAD v2:
17-42426535-G-A
PubMed:
PMID:16862115
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44349167G>A , CM000679.2:g.44349167G>A | GRCh38 |
| NC_000017.10:g.42426535G>A , CM000679.1:g.42426535G>A | GRCh37 |
| NC_000017.9:g.39782061G>A | NCBI36 |
| NG_007886.1:g.9045G>A , LRG_661:g.9045G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000053867.8:c.3G>A MANE Select | ENSP00000053867.2:p.Met1Ile | |
| ENST00000639447.1:c.3G>A | ENSP00000492014.1:p.Met1Ile | |
| ENST00000053867.7:c.3G>A | ENSP00000053867.2:p.Met1Ile | |
| ENST00000585512.5:c.3G>A | ENSP00000467745.1:p.Met1Ile | |
| ENST00000586782.5:c.3G>A | ENSP00000468318.1:p.Met1Ile | |
| ENST00000587109.5:c.3G>A | ENSP00000466271.1:p.Met1Ile | |
| ENST00000587387.5:c.3G>A | ENSP00000467431.1:p.Met1Ile | |
| ENST00000587518.5:c.3G>A | ENSP00000465518.1:p.Met1Ile | |
| ENST00000587958.1:n.39G>A | ||
| ENST00000588143.5:c.3G>A | ENSP00000465375.1:p.Met1Ile | |
| ENST00000588170.5:n.99G>A | ||
| ENST00000588237.5:c.3G>A | ENSP00000466611.1:p.Met1Ile | |
| ENST00000589265.5:c.3G>A | ENSP00000467616.1:p.Met1Ile | |
| ENST00000589536.5:c.3G>A | ENSP00000466956.1:p.Met1Ile | |
| ENST00000591740.5:c.3G>A | ENSP00000467022.1:p.Met1Ile | |
| ENST00000592323.5:n.43G>A | ||
| ENST00000592783.5:c.3G>A | ENSP00000467870.1:p.Met1Ile | |
| ENST00000593167.5:c.3G>A | ENSP00000466405.1:p.Met1Ile | |
| NM_002087.3:c.3G>A | NP_002078.1:p.Met1Ile | |
| XM_005257253.1:c.3G>A | XP_005257310.1:p.Met1Ile | |
| XM_024450730.1:c.3G>A | XP_024306498.1:p.Met1Ile | |
| NM_002087.4:c.3G>A MANE Select | NP_002078.1:p.Met1Ile |