HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96251050C>G , CM000664.2:g.96251050C>G | GRCh38 |
NC_000002.11:g.96916788C>G , CM000664.1:g.96916788C>G | GRCh37 |
NC_000002.10:g.96280515C>G | NCBI36 |
NG_027695.1:g.19964G>C , LRG_528:g.19964G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258439.8:c.*2758G>C MANE Select | ENSP00000258439.3:n.*2758G>C | |
ENST00000258439.7:c.*2758G>C | ENSP00000258439.2:n.*2758G>C | |
NM_001193304.2:c.*2758G>C | NP_001180233.1:n.*2758G>C | |
NM_017849.3:c.*2758G>C , LRG_528t1:c.*2758G>C | NP_060319.1:n.*2758G>C | |
XM_017004450.1:c.*2059G>C | XP_016859939.1:n.*2059G>C | |
XM_017004452.1:c.*2758G>C | XP_016859941.1:n.*2758G>C | |
NM_001193304.3:c.*2758G>C | NP_001180233.1:n.*2758G>C | |
NM_017849.4:c.*2758G>C MANE Select | NP_060319.1:n.*2758G>C |