HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116173455T>A , CM000685.2:g.116173455T>A | GRCh38 |
NC_000023.10:g.115304708T>A , CM000685.1:g.115304708T>A | GRCh37 |
NC_000023.9:g.115218736T>A | NCBI36 |
NG_016326.1:g.7751T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.*83T>A MANE Select | ENSP00000360973.4:n.*83T>A | |
ENST00000371906.4:c.*83T>A | ENSP00000360973.4:n.*83T>A | |
NM_000686.4:c.*83T>A | NP_000677.2:n.*83T>A | |
XM_011537533.1:c.*83T>A | XP_011535835.1:n.*83T>A | |
NM_000686.5:c.*83T>A MANE Select | NP_000677.2:n.*83T>A | |
NM_001385624.1:c.*83T>A | NP_001372553.1:n.*83T>A |