HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60372287G= , CM000680.2:g.60372287G= | GRCh38 |
NC_000018.9:g.58039520G= , CM000680.1:g.58039520G= | GRCh37 |
NC_000018.8:g.56190500G= | NCBI36 |
NG_016441.1:g.5482C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.63C= MANE Select | ENSP00000299766.3:p.Tyr21= | |
ENST00000299766.4:c.63C= | ENSP00000299766.3:p.Tyr21= | |
NM_005912.2:c.63C= | NP_005903.2:p.Tyr21= | |
NM_005912.3:c.63C= MANE Select | NP_005903.2:p.Tyr21= |