Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868887G>A , CM000664.2:g.240868887G>A | GRCh38 |
| NC_000002.11:g.241808304G>A , CM000664.1:g.241808304G>A | GRCh37 |
| NC_000002.10:g.241456977G>A | NCBI36 |
| NG_008005.1:g.5143G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.22G>A MANE Select | ENSP00000302620.3:p.Val8Met | |
| ENST00000307503.3:c.22G>A | ENSP00000302620.3:p.Val8Met | |
| ENST00000472436.1:n.42G>A | ||
| NM_000030.2:c.22G>A | NP_000021.1:p.Val8Met | |
| XR_924060.1:n.405+1346C>T | ||
| NM_000030.3:c.22G>A MANE Select | NP_000021.1:p.Val8Met |