HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1104044A= , CM000681.2:g.1104044A= | GRCh38 |
NC_000019.9:g.1104043A= , CM000681.1:g.1104043A= | GRCh37 |
NC_000019.8:g.1055043A= | NCBI36 |
NG_050621.1:g.5119A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706713.1:c.1A= | ENSP00000516510.1:p.Met1= | |
ENST00000354171.13:c.1A= MANE Select | ENSP00000346103.7:p.Met1= | |
ENST00000589115.6:c.1A= | ENSP00000466872.3:p.Met1= | |
ENST00000354171.12:c.1A= | ENSP00000346103.7:p.Met1= | |
ENST00000589115.5:c.1A= | ENSP00000466872.2:p.Met1= | |
ENST00000616066.4:c.1A= | ENSP00000485000.1:p.Met1= | |
NM_001039847.2:c.1A= | NP_001034936.1:p.Met1= | |
NM_002085.4:c.1A= | NP_002076.2:p.Met1= | |
NM_001039847.3:c.1A= | NP_001034936.1:p.Met1= | |
NM_002085.5:c.1A= MANE Select | NP_002076.2:p.Met1= |