HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24800139C>T , CM000666.2:g.24800139C>T | GRCh38 |
NC_000004.11:g.24801761C>T , CM000666.1:g.24801761C>T | GRCh37 |
NC_000004.10:g.24410859C>T | NCBI36 |
NG_012213.1:g.9677C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382120.4:c.618C>T MANE Select | ENSP00000371554.3:p.Ala206= | |
ENST00000382120.3:c.618C>T | ENSP00000371554.3:p.Ala206= | |
NM_003102.2:c.618C>T | NP_003093.2:p.Ala206= | |
XR_427488.1:n.808C>T | ||
NM_003102.3:c.618C>T | NP_003093.2:p.Ala206= | |
NM_003102.4:c.618C>T MANE Select | NP_003093.2:p.Ala206= |