HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52492660A>T , CM000674.2:g.52492660A>T | GRCh38 |
NC_000012.11:g.52886444A>T , CM000674.1:g.52886444A>T | GRCh37 |
NC_000012.10:g.51172711A>T | NCBI36 |
NG_008298.1:g.5738T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.529T>A MANE Select | ENSP00000369317.3:p.Phe177Ile | |
ENST00000330722.6:c.529T>A | ENSP00000369317.3:p.Phe177Ile | |
ENST00000549898.5:n.50T>A | ||
NM_005554.3:c.529T>A | NP_005545.1:p.Phe177Ile | |
NM_005554.4:c.529T>A MANE Select | NP_005545.1:p.Phe177Ile |