Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168293214T>G , CM000663.2:g.168293214T>G | GRCh38 |
| NC_000001.10:g.168262452T>G , CM000663.1:g.168262452T>G | GRCh37 |
| NC_000001.9:g.166529076T>G | NCBI36 |
| NG_008244.1:g.17175T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367821.8:c.539T>G MANE Select | ENSP00000356795.3:p.Met180Arg | |
| ENST00000367821.7:c.539T>G | ENSP00000356795.3:p.Met180Arg | |
| ENST00000431969.5:c.336T>G | ||
| NM_005149.2:c.539T>G | NP_005140.1:p.Met180Arg | |
| NM_005149.3:c.539T>G MANE Select | NP_005140.1:p.Met180Arg |