MyVariant.info:
GRCh37
chr12:g.72372833C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71979053C>A , CM000674.2:g.71979053C>A | GRCh38 |
| NC_000012.11:g.72372833C>A , CM000674.1:g.72372833C>A | GRCh37 |
| NC_000012.10:g.70659100C>A | NCBI36 |
| NG_008279.1:g.45208C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333850.4:c.907C>A MANE Select | ENSP00000329093.3:p.Arg303= | |
| ENST00000333850.3:c.907C>A | ENSP00000329093.3:p.Arg303= | |
| NM_173353.3:c.907C>A | NP_775489.2:p.Arg303= | |
| XM_011537899.1:c.313C>A | XP_011536201.1:p.Arg105= | |
| NM_173353.4:c.907C>A MANE Select | NP_775489.2:p.Arg303= |