HGVS | Genome Assembly |
---|---|
NC_000005.10:g.63960064C>G , CM000667.2:g.63960064C>G | GRCh38 |
NC_000005.9:g.63255891C>G , CM000667.1:g.63255891C>G | GRCh37 |
NC_000005.8:g.63291647C>G | NCBI36 |
NG_032816.1:g.7229G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000323865.5:c.*387G>C MANE Select | ENSP00000316244.4:n.*387G>C | |
NM_000524.3:c.*387G>C | NP_000515.2:n.*387G>C | |
NM_000524.4:c.*387G>C MANE Select | NP_000515.2:n.*387G>C |