Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31541272G>A , CM000680.2:g.31541272G>A | GRCh38 |
| NC_000018.9:g.29121235G>A , CM000680.1:g.29121235G>A | GRCh37 |
| NC_000018.8:g.27375233G>A | NCBI36 |
| NG_007072.3:g.48031G>A , LRG_397:g.48031G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261590.13:c.1959G>A MANE Select | ENSP00000261590.8:p.Met653Ile | |
| ENST00000261590.12:c.1959G>A | ENSP00000261590.8:p.Met653Ile | |
| NM_001943.3:c.1959G>A , LRG_397t1:c.1959G>A | NP_001934.2:p.Met653Ile | |
| NM_001943.4:c.1959G>A | NP_001934.2:p.Met653Ile | |
| XM_024451095.1:c.1425G>A | XP_024306863.1:p.Met475Ile | |
| NM_001943.5:c.1959G>A MANE Select | NP_001934.2:p.Met653Ile |