HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7525071T>G , CM000681.2:g.7525071T>G | GRCh38 |
NC_000019.9:g.7589957T>G , CM000681.1:g.7589957T>G | GRCh37 |
NC_000019.8:g.7495957T>G | NCBI36 |
NG_015806.1:g.7462T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.142T>G MANE Select | ENSP00000264079.5:p.Phe48Val | |
ENST00000264079.10:c.142T>G | ENSP00000264079.5:p.Phe48Val | |
ENST00000394321.9:n.222T>G | ||
ENST00000596390.1:n.258T>G | ||
ENST00000601003.1:c.142T>G | ENSP00000469074.1:p.Phe48Val | |
NM_020533.2:c.142T>G | NP_065394.1:p.Phe48Val | |
NM_020533.3:c.142T>G MANE Select | NP_065394.1:p.Phe48Val |