HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1104049C>T , CM000681.2:g.1104049C>T | GRCh38 |
NC_000019.9:g.1104048C>T , CM000681.1:g.1104048C>T | GRCh37 |
NC_000019.8:g.1055048C>T | NCBI36 |
NG_050621.1:g.5124C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706713.1:c.6C>T | ENSP00000516510.1:p.Ser2= | |
ENST00000354171.13:c.6C>T MANE Select | ENSP00000346103.7:p.Ser2= | |
ENST00000589115.6:c.6C>T | ENSP00000466872.3:p.Ser2= | |
ENST00000354171.12:c.6C>T | ENSP00000346103.7:p.Ser2= | |
ENST00000589115.5:c.6C>T | ENSP00000466872.2:p.Ser2= | |
ENST00000616066.4:c.6C>T | ENSP00000485000.1:p.Ser2= | |
NM_001039847.2:c.6C>T | NP_001034936.1:p.Ser2= | |
NM_002085.4:c.6C>T | NP_002076.2:p.Ser2= | |
NM_001039847.3:c.6C>T | NP_001034936.1:p.Ser2= | |
NM_002085.5:c.6C>T MANE Select | NP_002076.2:p.Ser2= |