HGVS | Genome Assembly |
---|---|
NC_000005.10:g.138468946T>C , CM000667.2:g.138468946T>C | GRCh38 |
NC_000005.9:g.137804635T>C , CM000667.1:g.137804635T>C | GRCh37 |
NC_000005.8:g.137832534T>C | NCBI36 |
NG_021374.1:g.8455T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239938.5:c.*865T>C MANE Select | ENSP00000239938.4:n.*865T>C | |
ENST00000239938.4:c.*865T>C | ENSP00000239938.4:n.*865T>C | |
NM_001964.2:c.*865T>C | NP_001955.1:n.*865T>C | |
NM_001964.3:c.*865T>C MANE Select | NP_001955.1:n.*865T>C |