HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18785079G>A , CM000681.2:g.18785079G>A | GRCh38 |
NC_000019.9:g.18895889G>A , CM000681.1:g.18895889G>A | GRCh37 |
NC_000019.8:g.18756889G>A | NCBI36 |
NG_007070.1:g.11226C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1731C>T MANE Select | ENSP00000222271.2:p.Phe577= | |
ENST00000222271.6:c.1731C>T | ENSP00000222271.2:p.Phe577= | |
ENST00000425807.1:c.1572C>T | ENSP00000403792.1:p.Phe524= | |
ENST00000542601.6:c.1632C>T | ENSP00000439156.2:p.Phe544= | |
NM_000095.2:c.1731C>T | NP_000086.2:p.Phe577= | |
NM_000095.3:c.1731C>T MANE Select | NP_000086.2:p.Phe577= |