HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188996169A= , CM000664.2:g.188996169A= | GRCh38 |
NC_000002.11:g.189860895A= , CM000664.1:g.189860895A= | GRCh37 |
NC_000002.10:g.189569140A= | NCBI36 |
NG_007404.1:g.26797A= , LRG_3:g.26797A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.1554A= | ENSP00000415346.2:p.Pro518= | |
ENST00000304636.9:c.1653A= MANE Select | ENSP00000304408.4:p.Pro551= | |
ENST00000304636.7:c.1653A= | ENSP00000304408.3:p.Pro551= | |
ENST00000317840.9:c.1653A= | ENSP00000315243.6:p.Pro551= | |
NM_000090.3:c.1653A= , LRG_3t1:c.1653A= | NP_000081.1:p.Pro551= | |
NM_000090.4:c.1653A= MANE Select | NP_000081.2:p.Pro551= |