HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114044366G= , CM000672.2:g.114044366G= | GRCh38 |
NC_000010.10:g.115804125G= , CM000672.1:g.115804125G= | GRCh37 |
NC_000010.9:g.115794115G= | NCBI36 |
NG_012187.1:g.5320G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.234G= MANE Select | ENSP00000358301.2:p.Leu78= | |
ENST00000369295.3:c.234G= | ENSP00000358301.2:p.Leu78= | |
NM_000684.2:c.234G= | NP_000675.1:p.Leu78= | |
NM_000684.3:c.234G= MANE Select | NP_000675.1:p.Leu78= |