HGVS | Genome Assembly |
---|---|
NC_000011.10:g.86954855C= , CM000673.2:g.86954855C= | GRCh38 |
NC_000011.9:g.86665897C= , CM000673.1:g.86665897C= | GRCh37 |
NC_000011.8:g.86343545C= | NCBI36 |
NG_011752.1:g.5537G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000531380.2:c.231G= MANE Select | ENSP00000434034.1:p.Leu77= | |
ENST00000531380.1:c.231G= | ENSP00000434034.1:p.Leu77= | |
NM_012193.3:c.231G= | NP_036325.2:p.Leu77= | |
NM_012193.4:c.231G= MANE Select | NP_036325.2:p.Leu77= |