HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20888407G>A , CM000684.2:g.20888407G>A | GRCh38 |
NC_000022.10:g.21242695G>A , CM000684.1:g.21242695G>A | GRCh37 |
NC_000022.9:g.19572695G>A | NCBI36 |
NG_012152.1:g.34404G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*571G>A MANE Select | ENSP00000215730.6:n.*571G>A | |
ENST00000215730.11:c.*571G>A | ENSP00000215730.6:n.*571G>A | |
NM_004782.3:c.*571G>A | NP_004773.1:n.*571G>A | |
NM_004782.4:c.*571G>A MANE Select | NP_004773.1:n.*571G>A |