HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65964426T>C , CM000674.2:g.65964426T>C | GRCh38 |
NC_000012.11:g.66358206T>C , CM000674.1:g.66358206T>C | GRCh37 |
NC_000012.10:g.64644473T>C | NCBI36 |
NG_016296.1:g.144967T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000403681.7:c.*1134T>C MANE Select | ENSP00000384026.2:n.*1134T>C | |
ENST00000403681.6:c.*1134T>C | ENSP00000384026.2:n.*1134T>C | |
NM_003483.4:c.*1134T>C | NP_003474.1:n.*1134T>C | |
NM_003483.6:c.*1134T>C MANE Select | NP_003474.1:n.*1134T>C |