HGVS | Genome Assembly |
---|---|
NC_000005.10:g.141331038T>C , CM000667.2:g.141331038T>C | GRCh38 |
NC_000005.9:g.140710605T>C , CM000667.1:g.140710605T>C | GRCh37 |
NC_000005.8:g.140690789T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517417.3:c.354T>C MANE Select | ENSP00000431083.1:p.Pro118= | |
ENST00000378105.4:c.354T>C | ENSP00000367345.3:p.Pro118= | |
ENST00000517417.2:c.354T>C | ENSP00000431083.1:p.Pro118= | |
NM_018912.2:c.354T>C | NP_061735.1:p.Pro118= | |
NM_031993.1:c.354T>C | NP_114382.1:p.Pro118= | |
NM_018912.3:c.354T>C MANE Select | NP_061735.1:p.Pro118= | |
NM_031993.2:c.354T>C | NP_114382.1:p.Pro118= |