HGVS | Genome Assembly |
---|---|
NC_000017.11:g.48530455C>T , CM000679.2:g.48530455C>T | GRCh38 |
NC_000017.10:g.46607817C>T , CM000679.1:g.46607817C>T | GRCh37 |
NC_000017.9:g.43962816C>T | NCBI36 |
NG_032884.1:g.5456G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239174.7:c.450G>A MANE Select | ENSP00000355140.5:p.Ala150= | |
ENST00000239174.6:c.450G>A | ENSP00000355140.5:p.Ala150= | |
ENST00000577092.1:c.450G>A | ENSP00000459066.1:p.Ala150= | |
NM_002144.3:c.450G>A | NP_002135.2:p.Ala150= | |
NM_002144.4:c.450G>A MANE Select | NP_002135.2:p.Ala150= |