HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218882195C= , CM000664.2:g.218882195C= | GRCh38 |
NC_000002.11:g.219746917C= , CM000664.1:g.219746917C= | GRCh37 |
NC_000002.10:g.219455161C= | NCBI36 |
NG_012179.1:g.6663C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258411.8:c.148C= MANE Select | ENSP00000258411.3:p.Pro50= | |
ENST00000258411.7:c.148C= | ENSP00000258411.3:p.Pro50= | |
ENST00000458582.1:c.35C= | ||
NM_025216.2:c.148C= | NP_079492.2:p.Pro50= | |
XM_011511928.1:c.97C= | XP_011510230.1:p.Pro33= | |
XM_011511929.1:c.52C= | XP_011510231.1:p.Pro18= | |
XM_011511930.1:c.148C= | XP_011510232.1:p.Pro50= | |
XM_011511929.2:c.52C= | XP_011510231.1:p.Pro18= | |
NM_025216.3:c.148C= MANE Select | NP_079492.2:p.Pro50= |