HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233231A>T , CM000667.2:g.55233231A>T | GRCh38 |
NC_000005.9:g.54529059A>T , CM000667.1:g.54529059A>T | GRCh37 |
NC_000005.8:g.54564816A>T | NCBI36 |
NG_034201.1:g.5487T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.293T>A MANE Select | ENSP00000282572.4:p.Phe98Tyr | |
ENST00000282572.4:c.293T>A | ENSP00000282572.4:p.Phe98Tyr | |
ENST00000501463.2:c.293T>A | ENSP00000422485.1:p.Phe98Tyr | |
NM_021147.4:c.293T>A | NP_066970.3:p.Phe98Tyr | |
NR_125346.1:n.487T>A | ||
NR_125347.1:n.487T>A | ||
NM_021147.5:c.293T>A MANE Select | NP_066970.3:p.Phe98Tyr | |
NR_125346.2:n.378T>A | ||
NR_125347.2:n.378T>A |