HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64759703C>A , CM000673.2:g.64759703C>A | GRCh38 |
NC_000011.9:g.64527175C>A , CM000673.1:g.64527175C>A | GRCh37 |
NC_000011.8:g.64283751C>A | NCBI36 |
NG_013018.1:g.6013G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.196G>T MANE Select | ENSP00000164139.3:p.Gly66Trp | |
ENST00000164139.3:c.196G>T | ENSP00000164139.3:p.Gly66Trp | |
ENST00000377432.7:c.196G>T | ENSP00000366650.3:p.Gly66Trp | |
NM_001164716.1:c.196G>T | NP_001158188.1:p.Gly66Trp | |
NM_005609.2:c.196G>T | NP_005600.1:p.Gly66Trp | |
NM_005609.3:c.196G>T | NP_005600.1:p.Gly66Trp | |
NM_005609.4:c.196G>T MANE Select | NP_005600.1:p.Gly66Trp |