HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122509065T>C , CM000672.2:g.122509065T>C | GRCh38 |
NC_000010.10:g.124268581T>C , CM000672.1:g.124268581T>C | GRCh37 |
NC_000010.9:g.124258571T>C | NCBI36 |
NG_011554.1:g.52541T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.1120+295T>C MANE Select | ENSP00000357980.3:n.1120+295T>C | |
ENST00000648167.1:c.802+295T>C | ENSP00000498033.1:n.802+295T>C | |
ENST00000368984.7:c.1120+295T>C | ENSP00000357980.3:n.1120+295T>C | |
ENST00000420892.1:c.343+295T>C | ENSP00000412676.1:n.343+295T>C | |
NM_002775.4:c.1120+295T>C | NP_002766.1:n.1120+295T>C | |
NM_002775.5:c.1120+295T>C MANE Select | NP_002766.1:n.1120+295T>C |