HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114044190G= , CM000672.2:g.114044190G= | GRCh38 |
NC_000010.10:g.115803949G= , CM000672.1:g.115803949G= | GRCh37 |
NC_000010.9:g.115793939G= | NCBI36 |
NG_012187.1:g.5144G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369295.4:c.58G= MANE Select | ENSP00000358301.2:p.Ala20= | |
ENST00000369295.3:c.58G= | ENSP00000358301.2:p.Ala20= | |
NM_000684.2:c.58G= | NP_000675.1:p.Ala20= | |
NM_000684.3:c.58G= MANE Select | NP_000675.1:p.Ala20= |