Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33850979G>C , CM000682.2:g.33850979G>C | GRCh38 |
| NC_000020.10:g.32438785G>C , CM000682.1:g.32438785G>C | GRCh37 |
| NC_000020.9:g.31902446G>C | NCBI36 |
| NG_015820.1:g.44676G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000217402.3:c.396G>C MANE Select | ENSP00000217402.2:p.Met132Ile | |
| ENST00000217402.2:c.396G>C | ENSP00000217402.2:p.Met132Ile | |
| NM_176812.4:c.396G>C | NP_789782.1:p.Met132Ile | |
| NM_176812.5:c.396G>C MANE Select | NP_789782.1:p.Met132Ile |