Linked Data
ClinVar Variation Id:
318938
ClinVar RCV Id:
RCV000290732
dbSNP Id:
rs886051911
gnomAD v4:
16-30753449-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30753449G>A , CM000678.2:g.30753449G>A | GRCh38 |
| NC_000016.9:g.30764770G>A , CM000678.1:g.30764770G>A | GRCh37 |
| NC_000016.8:g.30672271G>A | NCBI36 |
| NG_016616.1:g.10151G>A | |
| NG_016616.2:g.10151G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563588.6:c.448G>A MANE Select | ENSP00000455607.1:p.Val150Met | |
| ENST00000328273.11:c.448G>A | ENSP00000329968.7:p.Val150Met | |
| ENST00000424889.7:c.448G>A | ENSP00000388571.3:p.Val150Met | |
| ENST00000561712.1:c.122G>A | ||
| ENST00000563588.5:c.448G>A | ENSP00000455607.1:p.Val150Met | |
| ENST00000563607.1:c.*120G>A | ENSP00000454641.1:n.*120G>A | |
| ENST00000563913.5:n.781G>A | ||
| ENST00000564838.5:n.822G>A | ||
| ENST00000565897.5:c.448G>A | ENSP00000457359.1:p.Val150Met | |
| ENST00000565924.5:c.448G>A | ENSP00000455091.1:p.Val150Met | |
| ENST00000569684.1:n.860G>A | ||
| NM_000294.2:c.448G>A | NP_000285.1:p.Val150Met | |
| NM_001172432.1:c.448G>A | NP_001165903.1:p.Val150Met | |
| NM_000294.3:c.448G>A MANE Select | NP_000285.1:p.Val150Met | |
| NM_001172432.2:c.448G>A | NP_001165903.1:p.Val150Met |