HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155134221G>C , CM000663.2:g.155134221G>C | GRCh38 |
NC_000001.10:g.155106697G>C , CM000663.1:g.155106697G>C | GRCh37 |
NC_000001.9:g.153373321G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368407.8:c.*154G>C MANE Select | ENSP00000357392.3:n.*154G>C | |
ENST00000368406.2:c.*154G>C | ENSP00000357391.2:n.*154G>C | |
ENST00000368407.7:c.*154G>C | ENSP00000357392.3:n.*154G>C | |
ENST00000469878.5:n.1023G>C | ||
ENST00000474413.5:n.997G>C | ||
NM_004428.2:c.*154G>C | NP_004419.2:n.*154G>C | |
NM_182685.1:c.*154G>C | NP_872626.1:n.*154G>C | |
XM_005244940.3:c.*154G>C | XP_005244997.1:n.*154G>C | |
NM_004428.3:c.*154G>C MANE Select | NP_004419.2:n.*154G>C | |
NM_182685.2:c.*154G>C | NP_872626.1:n.*154G>C |