HGVS | Genome Assembly |
---|---|
NC_000015.10:g.45103963A>T , CM000677.2:g.45103963A>T | GRCh38 |
NC_000015.9:g.45396161A>T , CM000677.1:g.45396161A>T | GRCh37 |
NC_000015.8:g.43183453A>T | NCBI36 |
NG_009447.1:g.15199T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389039.11:c.2651T>A MANE Select | ENSP00000373691.7:p.Met884Lys | |
ENST00000389039.10:c.2651T>A | ENSP00000373691.6:p.Met884Lys | |
ENST00000558383.1:n.4382T>A | ||
ENST00000603300.1:c.2651T>A | ENSP00000475084.1:p.Met884Lys | |
NM_014080.4:c.2651T>A | NP_054799.4:p.Met884Lys | |
XM_005254421.2:c.2651T>A | XP_005254478.1:p.Met884Lys | |
NM_001363711.1:c.2651T>A | NP_001350640.1:p.Met884Lys | |
NM_001363711.2:c.2651T>A MANE Select | NP_001350640.1:p.Met884Lys | |
NM_014080.5:c.2651T>A | NP_054799.4:p.Met884Lys |