HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20888403C>T , CM000684.2:g.20888403C>T | GRCh38 |
NC_000022.10:g.21242691C>T , CM000684.1:g.21242691C>T | GRCh37 |
NC_000022.9:g.19572691C>T | NCBI36 |
NG_012152.1:g.34400C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*567C>T MANE Select | ENSP00000215730.6:n.*567C>T | |
ENST00000215730.11:c.*567C>T | ENSP00000215730.6:n.*567C>T | |
NM_004782.3:c.*567C>T | NP_004773.1:n.*567C>T | |
NM_004782.4:c.*567C>T MANE Select | NP_004773.1:n.*567C>T |