HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22812893C>G , CM000669.2:g.22812893C>G | GRCh38 |
NC_000007.13:g.22852512C>G , CM000669.1:g.22852512C>G | GRCh37 |
NC_000007.12:g.22819037C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000358435.8:c.*277G>C | ENSP00000351214.4:n.*277G>C | |
ENST00000463284.2:n.466G>C | ||
NM_019059.3:c.*277G>C | NP_061932.1:n.*277G>C | |
NM_019059.4:c.*277G>C | NP_061932.1:n.*277G>C |