HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23191863A>T , CM000670.2:g.23191863A>T | GRCh38 |
NC_000008.10:g.23049376A>T , CM000670.1:g.23049376A>T | GRCh37 |
NC_000008.9:g.23105321A>T | NCBI36 |
NG_032107.1:g.38305T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221132.8:c.1238T>A MANE Select | ENSP00000221132.3:p.Met413Lys | |
ENST00000221132.7:c.1238T>A | ENSP00000221132.3:p.Met413Lys | |
ENST00000519862.1:n.293T>A | ||
ENST00000613472.1:c.764T>A | ENSP00000480778.1:p.Met255Lys | |
NM_003844.3:c.1238T>A | NP_003835.3:p.Met413Lys | |
NM_003844.4:c.1238T>A MANE Select | NP_003835.3:p.Met413Lys |