HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174724599G>C , CM000667.2:g.174724599G>C | GRCh38 |
NC_000005.9:g.174151602G>C , CM000667.1:g.174151602G>C | GRCh37 |
NC_000005.8:g.174084208G>C | NCBI36 |
NG_008124.1:g.5028G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239243.7:c.-61G>C MANE Select | ENSP00000239243.5:n.-61G>C | |
ENST00000239243.6:c.-61G>C | ENSP00000239243.5:n.-61G>C | |
NM_002449.4:c.-61G>C | NP_002440.2:n.-61G>C | |
NM_001363626.1:c.-61G>C | NP_001350555.1:n.-61G>C | |
NM_002449.5:c.-61G>C MANE Select | NP_002440.2:n.-61G>C | |
NM_001363626.2:c.-61G>C | NP_001350555.1:n.-61G>C |