HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188994287A= , CM000664.2:g.188994287A= | GRCh38 |
NC_000002.11:g.189859013A= , CM000664.1:g.189859013A= | GRCh37 |
NC_000002.10:g.189567258A= | NCBI36 |
NG_007404.1:g.24915A= , LRG_3:g.24915A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.1149A= | ENSP00000415346.2:p.Pro383= | |
ENST00000304636.9:c.1248A= MANE Select | ENSP00000304408.4:p.Pro416= | |
ENST00000304636.7:c.1248A= | ENSP00000304408.3:p.Pro416= | |
ENST00000317840.9:c.1248A= | ENSP00000315243.6:p.Pro416= | |
ENST00000450867.1:c.247A= | ||
NM_000090.3:c.1248A= , LRG_3t1:c.1248A= | NP_000081.1:p.Pro416= | |
NM_000090.4:c.1248A= MANE Select | NP_000081.2:p.Pro416= |