HGVS | Genome Assembly |
---|---|
NC_000023.11:g.29917550T>A , CM000685.2:g.29917550T>A | GRCh38 |
NC_000023.10:g.29935667T>A , CM000685.1:g.29935667T>A | GRCh37 |
NC_000023.9:g.29845588T>A | NCBI36 |
NG_008292.1:g.1334987T>A | |
NG_008292.2:g.1334987T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378993.6:c.865T>A MANE Select | ENSP00000368278.1:p.Phe289Ile | |
ENST00000302196.5:c.88T>A | ENSP00000305200.5:p.Phe30Ile | |
ENST00000378993.5:c.865T>A | ENSP00000368278.1:p.Phe289Ile | |
NM_014271.3:c.865T>A | NP_055086.1:p.Phe289Ile | |
XM_005274441.1:c.865T>A | XP_005274498.1:p.Phe289Ile | |
XM_011545445.1:c.865T>A | XP_011543747.1:p.Phe289Ile | |
XM_017029240.1:c.865T>A | XP_016884729.1:p.Phe289Ile | |
XM_017029241.1:c.487T>A | XP_016884730.1:p.Phe163Ile | |
NM_014271.4:c.865T>A MANE Select | NP_055086.1:p.Phe289Ile |