Linked Data
gnomAD v4:
2-218814088-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814088A>C , CM000664.2:g.218814088A>C | GRCh38 |
| NC_000002.11:g.219678811A>C , CM000664.1:g.219678811A>C | GRCh37 |
| NC_000002.10:g.219387055A>C | NCBI36 |
| NG_007959.1:g.37340A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1085A>C MANE Select | ENSP00000258415.4:p.His362Pro | |
| ENST00000258415.8:c.1085A>C | ENSP00000258415.4:p.His362Pro | |
| ENST00000466602.1:n.1207A>C | ||
| ENST00000494263.5:n.1519A>C | ||
| NM_000784.3:c.1085A>C | NP_000775.1:p.His362Pro | |
| XM_017003488.2:c.665A>C | XP_016858977.1:p.His222Pro | |
| NM_000784.4:c.1085A>C MANE Select | NP_000775.1:p.His362Pro |