HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114044218C= , CM000672.2:g.114044218C= | GRCh38 |
NC_000010.10:g.115803977C= , CM000672.1:g.115803977C= | GRCh37 |
NC_000010.9:g.115793967C= | NCBI36 |
NG_012187.1:g.5172C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.86C= MANE Select | ENSP00000358301.2:p.Ala29= | |
ENST00000369295.3:c.86C= | ENSP00000358301.2:p.Ala29= | |
NM_000684.2:c.86C= | NP_000675.1:p.Ala29= | |
NM_000684.3:c.86C= MANE Select | NP_000675.1:p.Ala29= |