HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20888110T>G , CM000684.2:g.20888110T>G | GRCh38 |
NC_000022.10:g.21242398T>G , CM000684.1:g.21242398T>G | GRCh37 |
NC_000022.9:g.19572398T>G | NCBI36 |
NG_012152.1:g.34107T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*274T>G MANE Select | ENSP00000215730.6:n.*274T>G | |
ENST00000215730.11:c.*274T>G | ENSP00000215730.6:n.*274T>G | |
NM_004782.3:c.*274T>G | NP_004773.1:n.*274T>G | |
NM_004782.4:c.*274T>G MANE Select | NP_004773.1:n.*274T>G |