HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118304582T>C , CM000673.2:g.118304582T>C | GRCh38 |
NC_000011.9:g.118175297T>C , CM000673.1:g.118175297T>C | GRCh37 |
NC_000011.8:g.117680507T>C | NCBI36 |
NG_007383.1:g.5003T>C , LRG_38:g.5003T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.8:c.-254T>C | ENSP00000354566.4:n.-254T>C | |
NM_000733.3:c.-254T>C , LRG_38t1:c.-254T>C | NP_000724.1:n.-254T>C |