HGVS | Genome Assembly |
---|---|
NC_000023.11:g.120469146C= , CM000685.2:g.120469146C= | GRCh38 |
NC_000023.10:g.119603001C= , CM000685.1:g.119603001C= | GRCh37 |
NC_000023.9:g.119487029C= | NCBI36 |
NG_007995.1:g.5204G= , LRG_749:g.5204G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706600.1:c.24G= | ENSP00000516464.1:p.Pro8= | |
ENST00000200639.9:c.24G= MANE Select | ENSP00000200639.4:p.Pro8= | |
ENST00000200639.8:c.24G= | ENSP00000200639.4:p.Pro8= | |
ENST00000371335.4:c.24G= | ENSP00000360386.4:p.Pro8= | |
ENST00000434600.6:c.24G= | ENSP00000408411.2:p.Pro8= | |
NM_001122606.1:c.24G= , LRG_749t3:c.24G= | NP_001116078.1:p.Pro8= | |
NM_002294.2:c.24G= , LRG_749t1:c.24G= | NP_002285.1:p.Pro8= | |
NM_013995.2:c.24G= , LRG_749t2:c.24G= | NP_054701.1:p.Pro8= | |
NM_002294.3:c.24G= MANE Select | NP_002285.1:p.Pro8= |