HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269987T= , CM000668.2:g.31269987T= | GRCh38 |
NC_000006.11:g.31237764T= , CM000668.1:g.31237764T= | GRCh37 |
NC_000006.10:g.31345743T= | NCBI36 |
NG_029422.2:g.7145A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.994A= MANE Select | ENSP00000365402.5:p.Met332= | |
ENST00000376228.9:c.994A= | ENSP00000365402.5:p.Met332= | |
ENST00000376237.8:c.*581A= | ENSP00000365412.4:n.*581A= | |
ENST00000383329.7:c.994A= | ENSP00000372819.3:p.Met332= | |
ENST00000470363.5:n.312A= | ||
ENST00000487245.5:n.1353A= | ||
NM_002117.5:c.994A= | NP_002108.4:p.Met332= | |
NM_002117.6:c.994A= MANE Select | NP_002108.4:p.Met332= |